Which DNA Test is Best?

If you’re reading this article, congratulations. You’re a savvy shopper and you’re doing some research before purchasing a DNA test. You’ve come to the right place.

The most common question I receive is asking which test is best to purchase. There is no one single best answer for everyone – it depends on your testing goals and your pocketbook.

Testing Goals

People who want to have their DNA tested have a goal in mind and seek results to utilize for their particular purpose. Today, in the Direct to Consumer (DTC) DNA market space, people have varied interests that fall into the general categories of genealogy and medical/health.

I’ve approached the question of “which test is best” by providing information grouped into testing goal categories.  I’ve compared the different vendors and tests from the perspective of someone who is looking to test for those purposes – and I’ve created separate sections of this article for each interest..

We will be discussing testing for:

  • Ethnicity – Who Am I? – Breakdown by Various World Regions
  • Adoption – Finding Missing Parents or Close Family
  • Genealogy – Cousin Matching and Ancestor Search/Verification
  • Medical/Health

We will be reviewing the following test types:

  • Autosomal
  • Y DNA (males only)
  • Mitochondrial DNA

I have included summary charts for each section, plus an additional chart for:

  • Additional Vendor Considerations

If you are looking to select one test, or have limited funds, or are looking to prioritize certain types of tests, you’ll want to read about each vendor, each type of test, and each testing goal category.

Each category reports information about the vendors and their products from a different perspective – and only you can decide which of these perspectives and features are most important to you.

You might want to read this short article for a quick overview of the 4 kinds of DNA used for genetic genealogy and DTC testing and how they differ.

The Big 3

Today, there are three major players in the DNA testing market, not in any particular order:

Each of these companies offers autosomal tests, but each vendor offers features that are unique. Family Tree DNA and 23andMe offer additional tests as well.

In addition to the Big 3, there are a couple of new kids on the block that I will mention where appropriate. There are also niche players for the more advanced genetic genealogist or serious researcher, and this article does not address advanced research.

In a nutshell, if you are serious genealogist, you will want to take all of the following tests to maximize your tools for solving genealogical puzzles. There is no one single test that does everything.

  • Full mitochondrial sequence that informs you about your matrilineal line (only) at Family Tree DNA.
  • Y DNA test (for males only) that informs you about your direct paternal (surname) line (only) at Family Tree DNA.
  • Family Finder, an autosomal test that provides ethnicity estimates and cousin matching at Family Tree DNA.
  • AncestryDNA, an autosomal test at Ancestry.com that provides ethnicity estimates and cousin matching. (Do not confuse this test with Ancestry by DNA, which is not the same test and does not provide the same features.)
  • 23andMe Ancestry Service test, an autosomal test that provides ethnicity estimates and cousin matching.

A Word About Third Party Tools

A number of third party tools exist, such as GedMatch and DNAGedcom.com, and while these tools are quite useful after testing, these vendors don’t provide tests. In order to use these sites, you must first take an autosomal DNA test from a testing vendor. This article focuses on selecting your DNA testing vendor based on your testing goals.

Let’s get started!

Ethnicity

Many people are drawn to DNA testing through commercials that promise to ‘tell you who you are.” While the allure is exciting, the reality is somewhat different.

Each of the major three vendors provide an ethnicity estimate based on your autosomal DNA test, and each of the three vendors will provide you with a different result.

Yep, same person, different ethnicity breakdowns.

Hopefully, the outcomes will be very similar, but that’s certainly not always the case. However, many people take one test and believe those results wholeheartedly. Please don’t. You may want to read Concepts – Calculating Ethnicity Percentages to see how varied my own ethnicity reports are at various vendors as compared to my known genealogy.

The technology for understanding “ethnicity” from a genetic perspective is still very new. Your ethnicity estimate is based on reference populations from around the world – today. People and populations move, and have moved, for hundreds, thousands and tens of thousands of years. Written history only reaches back a fraction of that time, so the estimates provided to people today are not exact.

That isn’t to criticize any individual vendor. View each vendor’s results not as gospel, but as their opinion based on their reference populations and their internal proprietary algorithm of utilizing those reference populations to produce your ethnicity results.

To read more about how ethnicity testing works, and why your results may vary between vendors or not be what you expected, click here.

I don’t want to discourage anyone from testing, only to be sure consumers understand the context of what they will be receiving. Generally speaking, these results are accurate at the continental level, and less accurate within continents, such as European regional breakdowns.

All three testing companies provide additional features or tools, in addition to your ethnicity estimates, that are relevant to ethnicity or population groups.

Let’s look at each company separately.

Ethnicity – Family Tree DNA

Family Tree DNA’s ethnicity tool is called myOrigins and provides three features or tools in addition to the actual ethnicity estimate and associated ethnicity map.

Please note that throughout this article you can click on any image to enlarge.

On the myOrigins ethnicity map page, above, your ethnicity percentages and map are shown, along with two additional features.

The Shared Origins box to the left shows the matching ethnic components of people on your DNA match list. This is particularly useful if you are trying to discover, for example, where a particular minority admixture comes from in your lineage. You can select different match types, for example, immediate relatives or X chromosome matches, which have special inheritance qualities.

Clicking on the apricot (mitochondrial DNA) and green (Y DNA) pins in the lower right corner drops the pins in the locations on your map of the most distant ancestral Y and mitochondrial DNA locations of the individuals in the group you have selected in the Shared Origins match box. You may or may not match these individuals on the Y or mtDNA lines, but families tend to migrate in groups, so match hints of any kind are important.

A third unique feature provided by Family Tree DNA is Ancient Origins, a tool released with little fanfare in November 2016.

Ancient Origins shows the ancient source of your European DNA, based on genome sequencing of ancient DNA from the locations shown on the map.

Additionally, Family Tree DNA hosts an Ancient DNA project where they have facilitated the upload of the ancient genomes so that customers today can determine if they match these ancient individuals.

Kits included in the Ancient DNA project are shown in the chart below, along with their age and burial location. Some have matches today, and some of these samples are included on the Ancient Origins map.

Individual Approx. Age Burial Location Matches Ancient Origins Map
Clovis Anzick 12,500 Montana (US) Yes No
Linearbandkeramik 7,500 Stuttgart, Germany Yes Yes
Loschbour 8,000 Luxembourg Yes Yes
Palaeo-Eskimo 4,000 Greenland No No
Altai Neanderthal 50,000 Altai No No
Denisova 30,000 Siberia No No
Hinxton-4 2,000 Cambridgeshire, UK No No
BR2 3,200 Hungary Yes Yes
Ust’-Ishim 45,000 Siberia Yes No
NE1 7,500 Hungary Yes Yes

Ethnicity – Ancestry

In addition to your ethnicity estimate, Ancestry also provides a feature called Genetic Communities.

Your ethnicity estimate provides percentages of DNA found in regions shown on the map by fully colored shapes – green in Europe in the example above. Genetic Communities show how your DNA clusters with other people in specific regions of the world – shown with dotted clusters in the US in this example.

In my case, my ethnicity at Ancestry shows my European roots, illustrated by the green highlighted areas, and my two Genetic Communities are shown by yellow and red dotted regions in the United States.

My assigned Genetic Communities indicate that my DNA clusters with other people whose ancestors lived in two regions; The Lower Midwest and Virginia as well as the Alleghenies and Northeast Indiana.

Testers can then view their DNA matches within that community, as well as a group of surnames common within that community.

The Genetic Communities provided for me are accurate, but don’t expect all of your genealogical regions to be represented in Genetic Communities. For example, my DNA is 25% German, and I don’t have any German communities today, although ancestry will be adding new Genetic Communities as new clusters are formed.

You can read more about Genetic Communities here and here.

Ethnicity – 23andMe

In addition to ethnicity percentage estimates, called Ancestry Composition, 23andMe offers the ability to compare your Ancestry Composition against that of your parent to see which portions of your ethnicity you inherited from each parent, although there are problems with this tool incorrectly assigning parental segments.

Additionally, 23andMe paints your chromosome segments with your ethnic heritage, as shown below.

You can see that my yellow Native American segments appear on chromosomes 1 and 2.

In January 2017, 23andMe introduced their Ancestry Timeline, which I find to be extremely misleading and inaccurate. On my timeline, shown below, they estimate that my most recent British and Irish ancestor was found in my tree between 1900 and 1930 while in reality my most recent British/Irish individual found in my tree was born in England in 1759.

I do not view 23andMe’s Ancestry Timeline as a benefit to the genealogist, having found that it causes people to draw very misleading conclusions, even to the point of questioning their parentage based on the results. I wrote about their Ancestry Timeline here.

Ethnicity Summary

All three vendors provide both ethnicity percentage estimates and maps. All three vendors provide additional tools and features relevant to ethnicity. Vendors also provide matching to other people which may or may not be of interest to people who test only for ethnicity. “Who you are” only begins with ethnicity estimates.

DNA test costs are similar, although the Family Tree DNA test is less at $79. All three vendors have sales from time to time.

Ethnicity Vendor Summary Chart

Ethnicity testing is an autosomal DNA test and is available for both males and females.

Family Tree DNA Ancestry 23andMe
Ethnicity Test Included with $79 Family Finder test Included with $99 Ancestry DNA test Included with $99 Ancestry Service
Percentages and Maps Yes Yes Yes
Shared Ethnicity with Matches Yes No Yes
Additional Feature Y and mtDNA mapping of ethnicity matches Genetic Communities Ethnicity phasing against parent (has issues)
Additional Feature Ancient Origins Ethnicity mapping by chromosome
Additional Feature Ancient DNA Project Ancestry Timeline

 

Adoption and Parental Identity

DNA testing is extremely popular among adoptees and others in search of missing parents and grandparents.

The techniques used for adoption and parental search are somewhat different than those used for more traditional genealogy, although non-adoptees may wish to continue to read this section because many of the features that are important to adoptees are important to other testers as well.

Adoptees often utilize autosomal DNA somewhat differently than traditional genealogists by using a technique called mirror trees. In essence, the adoptee utilizes the trees posted online of their closest DNA matches to search for common family lines within those trees. The common family lines will eventually lead to the individuals within those common trees that are candidates to be the parents of the searcher.

Here’s a simplified hypothetical example of my tree and a first cousin adoptee match.

The adoptee matches me at a first cousin level, meaning that we share at least one common grandparent – but which one? Looking at other people the adoptee matches, or the adoptee and I both match, we find Edith Lore (or her ancestors) in the tree of multiple matches. Since Edith Lore is my grandmother, the adoptee is predicted to be my first cousin, and Edith Lore’s ancestors appear in the trees of our common matches – that tells us that Edith Lore is also the (probable) grandmother of the adoptee.

Looking at the possibilities for how Edith Lore can fit into the tree of me and the adoptee, as first cousins, we fine the following scenario.

Testing the known child of daughter Ferverda will then provide confirmation of this relationship if the known child proves to be a half sibling to the adoptee.

Therefore, close matches, the ability to contact matches and trees are very important to adoptees. I recommend that adoptees make contact with www.dnaadoption.com. The volunteers there specialize in adoptions and adoptees, provide search angels to help people and classes to teach adoptees how to utilize the techniques unique to adoption search such as building mirror trees.

For adoptees, the first rule is to test with all 3 major vendors plus MyHeritage. Family Tree DNA allows you to test with both 23andMe and Ancestry and subsequently transfer your results to Family Tree DNA, but I would strongly suggest adoptees test on the Family Tree DNA platform instead. Your match results from transferring to Family Tree DNA from other companies, except for MyHeritage, will be fewer and less reliable because both 23andMe and Ancestry utilize different chip technology.

For most genealogists, MyHeritage is not a player, as they have only recently entered the testing arena, have a very small data base, no tools and are having matching issues. I recently wrote about MyHeritage here. However, adoptees may want to test with MyHeritage, or upload your results to MyHeritage if you tested with Family Tree DNA, because your important puzzle-solving match just might have tested there and no place else. You can read about transfer kit compatibility and who accepts which vendors’ tests here.

Adoptees can benefit from ethnicity estimates at the continental level, meaning that regional (within continent) or minority ethnicity should be taken with a very large grain of salt. However, knowing that you have 25% Jewish heritage, for example, can be a very big clue to an adoptee’s search.

Another aspect of the adoptees search that can be relevant is the number of foreign testers. For many years, neither 23andMe, nor Ancestry tested substantially (or at all) outside the US. Family Tree DNA has always tested internationally and has a very strong Jewish data base component.

Not all vendors report X chromosome matches. The X chromosome is important to genetic genealogy, because it has a unique inheritance path. Men don’t inherit an X chromosome from their fathers. Therefore, if you match someone on the X chromosome, you know the relationship, for a male, must be from their mother’s side. For a female, the relationship must be from the mother or the father’s mother’s side. You can read more about X chromosome matching here.

Neither Ancestry nor MyHeritage have chromosome browsers which allow you to view the segments of DNA on which you match other individuals, which includes the X chromosome.

Adoptee Y and Mitochondrial Testing

In addition to autosomal DNA testing, adoptees will want to test their Y DNA (males only) and mitochondrial DNA.

These tests are different from autosomal DNA which tests the DNA you receive from all of your ancestors. Y and mitochondrial DNA focus on only one specific line, respectively. Y DNA is inherited by men from their fathers and the Y chromosome is passed from father to son from time immemorial. Therefore, testing the Y chromosome provides us with the ability to match to current people as well as to use the Y chromosome as a tool to look far back in time. Adoptees tend to be most interested in matching current people, at least initially.

Working with male adoptees, I have a found that about 30% of the time a male will match strongly to a particular surname, especially at higher marker levels. That isn’t always true, but adoptees will never know if they don’t test. An adoptee’s match list is shown at 111 markers, below.

Furthermore, utilizing the Y and mitochondrial DNA test in conjunction with autosomal DNA matching at Family Tree DNA helps narrows possible relatives. The Advanced Matching feature allows you to see who you match on both the Y (or mitochondrial) DNA lines AND the autosomal test, in combination.

Mitochondrial DNA tests the matrilineal line only, as women pass their mitochondrial DNA to all of their children, but only females pass it on. Family Tree DNA provides matching and advanced combination matching/searching for mitochondrial DNA as well as Y DNA. Both genders of children carry their mother’s mitochondrial DNA. Unfortunately, mitochondrial DNA is more difficult to work with because of the surname changes in each generation, but you cannot be descended from a woman, or her direct matrilineal ancestors if you don’t substantially match her mitochondrial DNA.

Some vendors state that you receive mitochondrial DNA with your autosomal results, which is only partly accurate. At 23andMe, you receive a haplogroup but no detailed results and no matching. 23andMe does not test the entire mitochondria and therefore cannot provide either advanced haplogroup placement nor Y or mitochondrial DNA matching between testers.

For additional details on the Y and Mitochondrial DNA tests themselves and what you receive, please see the Genealogy – Y and Mitochondrial DNA section.

Adoption Summary

Adoptees should test with all 4 vendors plus Y and mitochondrial DNA testing.

  • Ancestry – due to their extensive data base size and trees
  • Family Tree DNA – due to their advanced tools, chromosome browser, Y and mitochondrial DNA tests (Ancestry and 23andMe participants can transfer autosomal raw data files and see matches for free, but advanced tools require either an unlock fee or a test on the Family Tree DNA platform)
  • 23andMe – no trees and many people don’t participate in sharing genetic information
  • MyHeritage – new kid on the block, working through what is hoped are startup issues
  • All adoptees should take the full mitochondrial sequence test.
  • Male adoptees should take the 111 marker Y DNA test, although you can start with 37 or 67 markers and upgrade later.
  • Y and mitochondrial tests are only available at Family Tree DNA.

Adoptee Vendor Feature Summary Chart

Family Tree DNA Ancestry 23andMe MyHeritage
Autosomal DNA – Males and Females
Matching Yes Yes Yes Yes – problems
Relationship Estimates* Yes – May be too close Yes – May be too distant Yes – Matches may not be sharing Yes –  problematic
International Reach Very strong Not strong but growing Not strong Small but subscriber base is European focused
Trees Yes Yes No Yes
Tree Quantity 54% have trees, 46% no tree (of my first 100 matches) 56% have trees, 44% no tree or private (of my first 100 matches) No trees ~50% don’t have trees or are private (cannot discern private tree without clicking on every tree)
Data Base Size Large Largest Large – but not all opt in to matching Very small
My # of Matches on 4-23-2017 2,421 23,750 1,809 but only 1,114 are sharing 75
Subscription Required No No for partial, Yes for full functionality including access to matches’ trees, minimal subscription for $59 by calling Ancestry No No for partial, Yes for full functionality
Other Relevant Tools New Ancestor Discoveries
Autosomal DNA Issues Many testers don’t have trees Many testers don’t have trees Matching opt-in is problematic, no trees at all Matching issues, small data base size is problematic, many testers don’t have trees
Contact Methodology E-mail address provided to matches Internal message system – known delivery issues Internal message system Internal message system
X Chromosome Matching Yes No Yes No
Y-DNA – Males Only
Y DNA STR Test Yes- 37, 67, and 111 markers No No No
Y Haplogroup Yes as part of STR test plus additional testing available No Yes, basic level but no additional testing available, outdated haplogroups No
Y Matching Yes No No No
Advanced Matching Between Y and Autosomal Yes No No No
Mitochondrial DNA- Males and Females
Test Yes, partial and full sequence No No No
Mitochondrial DNA Haplogroup Yes, included in test No Yes, basic but full haplogroup not available, haplogroup several versions behind No
Advanced Matching Between Mitochondrial and Autosomal Yes No No No

Genealogy – Cousin Matching and Ancestor Search/Verification

People who want to take a DNA test to find cousins, to learn more about their genealogy, to verify their genealogy research or to search for unknown ancestors and break down brick walls will be interested in various types of testing

Test Type Who Can Test
Y DNA – direct paternal line Males only
Mitochondrial DNA – direct matrilineal line Males and Females
Autosomal – all lines Males and Females

Let’s begin with autosomal DNA testing for genealogy which tests your DNA inherited from all ancestral lines.

Aside from ethnicity, autosomal DNA testing provides matches to other people who have tested. A combination of trees, meaning their genealogy, and their chromosome segments are used to identify (through trees) and verify (through DNA segments) common ancestor(s) and then to assign a particular DNA segment(s) to that ancestor or ancestral couple. This process, called triangulation, then allows you to assign specific segments to particular ancestors, through segment matching among multiple people. You then know that when another individual matches you and those other people on the same segment, that the DNA comes from that same lineage. Triangulation is the only autosomal methodology to confirm ancestors who are not close relatives, beyond the past 2-3 generations or so.

All three vendors provide matching, but the tools they include and their user interfaces are quite different. 

Genealogy – Autosomal –  Family Tree DNA

Family Tree DNA entered DNA testing years before any of the others, initially with Y and mitochondrial DNA testing.

Because of the diversity of their products, their website is somewhat busier, but they do a good job of providing areas on the tester’s personal landing page for each of the products and within each product, a link for each feature or function.

For example, the Family Finder test is Family Tree DNA’s autosomal test. Within that product, tools provided are:

  • Matching
  • Chromosome Browser
  • Linked Relationships
  • myOrigins
  • Ancient Origins
  • Matrix
  • Advanced Matching

Unique autosomal tools provided by Family Tree DNA are:

  • Linked Relationships that allows you to connect individuals that you match to their location in your tree, indicating the proper relationship. Phased Family Matching uses these relationships within your tree to indicate which side of your tree other matches originate from.
  • Phased Family Matching shows which side of your tree, maternal, paternal or both, someone descends from, based on phased DNA matching between you and linked relationship matches as distant as third cousins. This allows Family Tree DNA to tell you whether matches are paternal (blue icon), maternal (red icon) or both (purple icon) without a parent’s DNA. This is one of the best autosomal tools at Family Tree DNA, shown below.

  • In Common With and Not In Common With features allow you to sort your matches in common with another individual a number of ways, or matches not in common with that individual.
  • Filtered downloads provide the downloading of chromosome data for your filtered match list.
  • Stackable filters and searches – for example, you can select paternal matches and then search for a particular surname or ancestral surname within the paternal matches.
  • Common ethnicity matching through myOrigins allows you to see selected groups of individuals who match you and share common ethnicities.
  • Y and mtDNA locations of autosomal matches are provided on your ethnicity map through myOrigins.
  • Advanced matching tool includes Y, mtDNA and autosomal in various combinations. Also includes matches within projects where the tester is a member as well as by partial surname.
  • The matrix tool allows the tester to enter multiple people that they match in order to see if those individuals also match each other. The matrix tool is, in combination with the in-common-with tool and the chromosome browser is a form of pseudo triangulation, but does not indicate that the individuals match on the same segment.

  • Chromosome browser with the ability to select different segment match thresholds to display when comparing 5 or fewer individuals to your results.
  • Projects to join which provide group interaction and allow individuals to match only within the project, if desired.

To read more about how to utilize the various autosomal tools at Family Tree DNA, with examples, click here.

Genealogy – Autosomal – Ancestry

Ancestry only offers autosomal DNA testing to their customers, so their page is simple and straightforward.

Ancestry is the only testing vendor (other than MyHeritage who is not included in this section) to require a subscription for full functionality, although if you call the Ancestry support line, a minimal subscription is available for $59. You can see your matches without a subscription, but you cannot see your matches trees or utilize other functions, so you will not be able to tell how you connect to your matches. Many genealogists have Ancestry subscriptions, so this is minimally problematic for most people.

However, if you don’t realize you need a subscription initially, the required annual subscription raises the effective cost of the test quite substantially. If you let your subscription lapse, you no longer have access to all DNA features. The cost of testing with Ancestry is the cost of the test plus the cost of a subscription if you aren’t already a subscriber.

This chart, from the Ancestry support center, provides details on which features are included for free and which are only available with a subscription.

Unique tools provided by Ancestry include:

  • Shared Ancestor Hints (green leaves) which indicate a match with whom you share a common ancestor in your tree connected to your DNA, allowing you to display the path of you and your match to the common ancestor. In order to take advantage of this feature, testers must link their tree to their DNA test. Otherwise, Ancestry can’t do tree matching.  As far as I’m concerned, this is the single most useful DNA tool at Ancestry. Subscription required.

  • DNA Circles, example below, are created when several people whose DNA matches also share a common ancestor. Subscription required.

  • New Ancestor Discoveries (NADs), which are similar to Circles, but are formed when you match people descended from a common ancestor, but don’t have that ancestor in your tree. The majority of the time, these NADs are incorrect and are, when dissected and the source can be determined, found to be something like the spouse of a sibling of your ancestor. I do not view NADs as a benefit, more like a wild goose chase, but for some people these could be useful so long as the individual understands that these are NOT definitely ancestors and only hints for research. Subscription required.
  • Ancestry uses a proprietary algorithm called Timber to strip DNA from you and your matches that they consider to be “too matchy,” with the idea that those segments are identical by population, meaning likely to be found in large numbers within a population group – making them meaningless for genealogy. The problem is that Timber results in the removal of valid segments, especially in endogamous groups like Acadian families. This function is unique to Ancestry, but many genealogists (me included) don’t consider Timber a benefit.
  • Genetic Communities shows you groups of individuals with whom your DNA clusters. The trees of cluster members are then examined by Ancestry to determine connections from which Genetic Communities are formed. You can filter your DNA match results by Genetic Community.

Genealogy – Autosomal – 23and Me

Unfortunately, the 23andMe website is not straightforward or intuitive. They have spent the majority of the past two years transitioning to a “New Experience” which has resulted in additional confusion and complications when matching between people on multiple different platforms. You can take a spin through the New Experience by clicking here.

23andMe requires people to opt-in to sharing, even after they have selected to participate in Ancestry Services (genealogy) testing, have opted-in previously and chosen to view their DNA Relatives. Users on the “New Experience” can then either share chromosome data and results with each other individually, meaning on a one by one basis, or globally by a one-time opt-in to “open sharing” with matches. If a user does not opt-in to both DNA Relatives and open sharing, sharing requests must be made individually to each match, and they must opt-in to share with each individual user. This complexity and confusion results in an approximate sharing rate of between 50 and 60%. One individual who religiously works their matches by requesting sharing now has a share rate of about 80% of their matches in the data base who HAVE initially selected to participate in DNA Relatives. You can read more about the 23andMe experience at this link.

Various genetic genealogy reports and tools are scattered between the Reports and Tools tabs, and within those, buried in non-intuitive locations. If you are going to utilize 23andMe for matching and genealogy, in addition to the above link, I recommend Kitty Cooper’s blogs about the new DNA Relatives here and on triangulation here. Print the articles, and use them as a guide while navigating the 23andMe site.

Note that some screens (the Tools, DNA Relatives, then DNA tab) on the site do not display/work correctly utilizing Internet Explorer, but do with Edge or other browsers.

The one genealogy feature unique to 23andMe is:

  • Triangulation at 23andMe allows you to select a specific match to compare your DNA against. Several pieces of information will be displayed, the last of which, scrolling to the bottom, is a list of your common relatives with the person you selected.

In the example below, I’ve selected to see the matches I match in common with known family member, Stacy Den (surnames have been obscured for privacy reasons.)  Please note that the Roberta V4 Estes kit is a second test that I took for comparison purposes when the new V4 version of 23andMe was released.  Just ignore that match, because, of course I match myself as a twin.

If an individual does not match both you and your selected match, they will not appear on this list.

In the “relatives in common” section, each person is listed with a “shared DNA” column. For a person to be shown on this “in common” list, you obviously do share DNA with these individuals and they also share with your match, but the “shared DNA” column goes one step further. This column indicates whether or not you and your match both share a common DNA segment with the “in common” person.

I know this is confusing, so I’ve created this chart to illustrate what will appear in the “Shared DNA” column of the individuals showing on the list of matches, above, shared between me and Stacy Den.

Clicking on “Share to see” sends Sarah a sharing request for her to allow you to see her segment matches.

Let’s look at an example with “yes” in the Shared DNA column.

Clicking on the “Yes” in the Shared DNA column of Debbie takes us to the chromosome browser which shows both your selected match, Stacy in my case, and Debbie, the person whose “yes” you clicked.

All three people, meaning me, Stacy and Debbie share a common DNA segment, shown below on chromosome 17.

What 23andMe does NOT say is that these people. Stacy and Debbie, also match each other, in addition to matching me, which means all three of us triangulate.

Because I manage Stacy’s kit at 23andMe, I can check to see if Debbie is on Stacy’s match list, and indeed, Debbie is on Stacy’s match list and Stacy does match both Debbie and me on chromosome 17 in exactly the same location shown above, proving unquestionably that the three of us all match each other and therefore triangulate on this segment. In our case, it’s easy to identify our common relative whose DNA all 3 of us share.

Genealogy – Autosomal Summary

While all 3 vendors offer matching, their interfaces and tools vary widely.

I would suggest that Ancestry is the least sophisticated and has worked hard to make their tools easy for the novice working with genetic genealogy. Their green leaf DNA+Tree Matching is their best feature, easy to use and important for the novice and experienced genealogist alike.  Now, if they just had that chromosome browser so we could see how we match those people.

Ancestry’s Circles, while a nice feature, encourage testers to believe that their DNA or relationship is confirmed by finding themselves in a Circle, which is not the case.

Circles can be formed as the result of misinformation in numerous trees. For example, if I were to inaccurately list Smith as the surname for one of my ancestor’s wives, I would find myself in a Circle for Barbara Smith, when in fact, there is absolutely no evidence whatsoever that her surname is Smith. Yet, people think that Barbara Smith is confirmed due to a Circle having been formed and finding themselves in Barbara Smith’s Circle. Copying incorrect trees equals the formation of incorrect Circles.

It’s also possible that I’m matching people on multiple lines and my DNA match to the people in any given Circle is through another common ancestor entirely.

A serious genealogist will test minimally at Ancestry and at Family Tree DNA, who provides a chromosome browser and other tools necessary to confirm relationships and shared DNA segments.

Family Tree DNA is more sophisticated, so consequently more complex to use.  They provide matching plus numerous other tools. The website and matching is certainly friendly for the novice, but to benefit fully, some experience or additional education is beneficial, not unlike traditional genealogy research itself. This is true not just for Family Tree DNA, but GedMatch and 23andMe who all three utilize chromosome browsers.

The user will want to understand what a chromosome browser is indicating about matching DNA segments, so some level of education makes life a lot easier. Fortunately, understanding chromosome browser matching is not complex. You can read an article about Match Groups and Triangulation here. I also have an entire series of Concepts articles, Family Tree DNA offers a webinar library, their Learning Center and other educational resources are available as well.

Family Tree DNA is the only vendor to provide Phased Family Matches, meaning that by connecting known relatives who have DNA tested to your tree, Family Tree DNA can then identify additional matches as maternal, paternal or both. This, in combination with pseudo-phasing are very powerful matching tools.

23andMe is the least friendly of the three companies, with several genetic genealogy unfriendly restrictions relative to matching, opt-ins, match limits and such. They have experienced problem after problem for years relative to genetic genealogy, which has always been a second-class citizen compared to their medical research, and not a priority.

23andMe has chosen to implement a business model where their customers must opt-in to share segment information with other individuals, either one by one or by opting into open sharing. Based on my match list, roughly 60% of my actual DNA matches have opted in to sharing.

Their customer base includes fewer serious genealogists and their customers often are not interested in genealogy at all.

Having said that, 23andMe is the only one of the three that provides actual triangulated matches for users on the New Experience and who have opted into sharing.

If I were entering the genetic genealogy testing space today, I would test my autosomal DNA at Ancestry and at Family Tree DNA, but I would probably not test at 23andMe. I would test both my Y DNA (if a male) and mitochondrial at Family Tree DNA.

Thank you to Kitty Cooper for assistance with parent/child matching and triangulation at 23andMe.

Genealogy Autosomal Vendor Feature Summary Chart

Family Tree DNA Ancestry 23andMe
Matching Yes Yes Yes – each person has to opt in for open sharing or authorize sharing individually, many don’t
Estimated Relationships Yes Yes Yes
Chromosome Browser Yes No – Large Issue Yes
Chromosome Browser Threshold Adjustment Yes No Chromosome Browser No
X Chromosome Matching Yes No Yes
Trees Yes Yes – subscription required so see matches’ trees No
Ability to upload Gedcom file Yes Yes No
Ability to search trees Yes Yes No
Subscription in addition to DNA test price No No for partial, Yes for full functionality, minimal subscription for $59 by calling Ancestry No
DNA + Ancestor in Tree Matches No Yes – Leaf Hints – subscription required – Best Feature No
Phased Parental Side Matching Yes – Best Feature No No
Parent Match Indicator Yes No Yes
Sort or Group by Parent Match Yes Yes Yes
In Common With Tool Yes Yes Yes
Not In Common With Tool Yes No No
Triangulated Matches No – pseudo with ICW, browser and matrix No Yes – Best Feature
Common Surnames Yes Yes – subscription required No
Ability to Link DNA Matches on Tree Yes No No
Matrix to show match grid between multiple matches Yes No No
Match Filter Tools Yes Minimal Some
Advanced Matching Tool Yes No No
Multiple Test Matching Tool Yes No multiple tests No multiple tests
Ethnicity Matching Yes No Yes
Projects Yes No No
Maximum # of Matches Restricted No No Yes – 2000 unless you are communicating with the individuals, then they are not removed from your match list
All Customers Participate Yes Yes, unless they don’t have a subscription No – between 50-60% opt-in
Accepts Transfers from Other Testing Companies Yes No No
Free Features with Transfer Matching, ICW, Matrix, Advanced Matching No transfers No transfers
Transfer Features Requiring Unlock $ Chromosome Browser, Ethnicity, Ancient Origins, Linked Relationships, Parentally Phased Matches No Transfers No transfers
Archives DNA for Later Testing Yes, 25 years No, no additional tests available No, no additional tests available
Additional Tool DNA Circles – subscription required
Additional Tool New Ancestor Discoveries – subscription required
Y DNA Not included in autosomal test but is additional test, detailed results including matching No Haplogroup only
Mitochondrial DNA Not included in autosomal test but is additional test, detailed results including matching No Haplogroup only
Advanced Testing Available Yes No No
Website Intuitive Yes, given their many tools Yes, very simple No
Data Base Size Large Largest Large but many do not test for genealogy, only test for health
Strengths Many tools, multiple types of tests, phased matching without parent DNA + Tree matching, size of data base Triangulation
Challenges Website episodically times out No chromosome browser or advanced tools Sharing is difficult to understand and many don’t, website is far from intuitive

 

Genealogy – Y and Mitochondrial DNA

Two indispensable tools for genetic genealogy that are often overlooked are Y and mitochondrial DNA.

The inheritance path for Y DNA is shown by the blue squares and the inheritance path for mitochondrial DNA is shown by the red circles for the male and female siblings shown at the bottom of the chart.

Y-DNA Testing for Males

Y DNA is inherited by males only, from their father. The Y chromosome makes males male. Women instead inherit an X chromosome from their father, which makes them female. Because the Y chromosome is not admixed with the DNA of the mother, the same Y chromosome has been passed down through time immemorial.

Given that the Y chromosome follows the typical surname path, Y DNA testing is very useful for confirming surname lineage to an expected direct paternal ancestor. In other words, an Estes male today should match, with perhaps a few mutations, to other descendants of Abraham Estes who was born in 1647 in Kent, England and immigrated to the colony of Virginia.

Furthermore, that same Y chromosome can look far back in time, thousands of years, to tell us where that English group of Estes men originated, before the advent of surnames and before the migration to England from continental Europe. I wrote about the Estes Y DNA here, so you can see an example of how Y DNA testing can be used.

Y DNA testing for matching and haplogroup identification, which indicates where in the world your ancestors were living within the past few hundred to few thousand years, is only available from Family Tree DNA. Testing can be purchased for either 37, 67 or 111 markers, with the higher marker numbers providing more granularity and specificity in matching.

Family Tree DNA provides three types of Y DNA tests.

  • STR (short tandem repeat) testing is the traditional Y DNA testing for males to match to each other in a genealogically relevant timeframe. These tests can be ordered in panels of 37, 67 or 111 markers and lower levels can be upgraded to higher levels at a later date. An accurate base haplogroup prediction is made from STR markers.
  • SNP (single nucleotide polymorphism) testing is a different type of testing that tests single locations for mutations in order to confirm and further refine haplogroups. Think of a haplogroup as a type of genetic clan, meaning that haplogroups are used to track migration of humans through time and geography, and are what is utilized to determine African, European, Asian or Native heritage in the direct paternal line. SNP tests are optional and can be ordered one at a time, in groups called panels for a particular haplogroup or a comprehensive research level Y DNA test called the Big Y can be ordered after STR testing.
  • The Big Y test is a research level test that scans the entire Y chromosome to determine the most refined haplogroup possible and to report any previously unknown mutations (SNPs) that may define further branches of the Y DNA tree. This is the technique used to expand the Y haplotree.

You can read more about haplogroups here and about the difference between STR markers and SNPs here, here and here.

Customers receive the following features and tools when they purchase a Y DNA test at Family Tree DNA or the Ancestry Services test at 23andMe. The 23andMe Y DNA information is included in their Ancestry Services test. The Family Tree DNA Y DNA information requires specific tests and is not included in the Family Finder test. You can click here to read about the difference in the technology between Y DNA testing at Family Tree DNA and at 23andMe. Ancestry is not included in this comparison because they provide no Y DNA related information.

Y DNA Vendor Feature Summary Chart

Family Tree DNA 23andMe
Varying levels of STR panel marker testing Yes, in panels of 37, 67 and 111 markers No
Test panel (STR) marker results Yes Not tested
Haplogroup assignment Yes – accurate estimate with STR panels, deeper testing available Yes –base haplogroup by scan – haplogroup designations are significantly out of date, no further testing available
SNP testing to further define haplogroup Yes – can purchase individual SNPs, by SNP panels or Big Y test No
Matching to other participants Yes No
Trees available for your matches Yes No
E-mail of matches provided Yes No
Calculator tool to estimate probability of generational distance between you and a match Yes No
Earliest known ancestor information Yes No
Projects Surname, haplogroup and geographic projects No
Ability to search Y matches Yes No Y matching
Ability to search matches within projects Yes No projects
Ability to search matches by partial surname Yes No
Haplotree and customer result location on tree Yes, detailed with every branch Yes, less detailed, subset
Terminal SNP used to determine haplogroup Yes Yes, small subset available
Haplogroup Map Migration map Heat map
Ancestral Origins – summary by ancestral location of others you match, by test level Yes No
Haplogroup Origins – match ancestral location summary by haplogroup, by test level Yes No
SNP map showing worldwide locations of any selected SNP Yes No
Matches map showing mapped locations of your matches most distant ancestor in the paternal line, by test panel Yes No
Big Y – full scan of Y chromosome for known and previously unknown mutations (SNPs) Yes No
Big Y matching Yes No
Big Y matching known SNPs Yes No
Big Y matching novel variants (unknown or yet unnamed SNPs) Yes No
Filter Big Y matches Yes No
Big Y results Yes No
Advanced matching for multiple test types Yes No
DNA is archived so additional tests or upgrades can be ordered at a later date Yes, 25 years No

Mitochondrial DNA Testing for Everyone

Mitochondrial DNA is contributed to both genders of children by mothers, but only the females pass it on. Like the Y chromosome, mitochondrial DNA is not admixed with the DNA of the other parent. Therefore, anyone can test for the mitochondrial DNA of their matrilineal line, meaning their mother’s mother’s mother’s lineage.

Matching can identify family lines as well as ancient lineage.

You receive the following features and tools when you purchase a mitochondrial DNA test from Family Tree DNA or the Ancestry Services test from 23andMe. The Family Tree DNA mitochondrial DNA information requires specific tests and is not included in the Family Finder test. The 23andMe mitochondrial information is provided with the Ancestry Services test. Ancestry is omitted from this comparison because they do not provide any mitochondrial information.

Mitochondrial DNA Vendor Feature Summary Chart

Family Tree DNA 23andMe
Varying levels of testing Yes, mtPlus and Full Sequence No
Test panel marker results Yes, in two formats, CRS and RSRS No
Rare mutations, missing and extra mutations, insertions and deletions reported Yes No
Haplogroup assignment Yes, most current version, Build 17 Yes, partial and out of date version
Matching to other participants Yes No
Trees of matches available to view Yes No
E-mail address provided to matches Yes No
Earliest known ancestor information Yes No
Projects Surname, haplogroup and geographic available No
Ability to search matches Yes No
Ability to search matches within project Yes No projects
Ability to search match by partial surname Yes No
Haplotree and customer location on tree No Yes
Mutations used to determine haplogroup provided Yes No
Haplogroup Map Migration map Heat map
Ancestral Origins – summary by ancestral location of others you match, by test level Yes No
Haplogroup Origins –match ancestral location summary by haplogroup Yes No
Matches map showing mapped locations of your matches most distant ancestor in the maternal line, by test level Yes No
Advanced matching for multiple test types Yes No
DNA is archived so additional tests or upgrades can be ordered at a later date Yes, 25 years No

 

Overall Genealogy Summary

Serious genealogists should test with at least two of the three major vendors, being Family Tree DNA and Ancestry, with 23andMe coming in as a distant third.

No genetic genealogy testing regimen is complete without Y and mitochondrial DNA for as many ancestral lines as you can find to test. You don’t know what you don’t know, and you’ll never know if you don’t test.

Unfortunately, many people, especially new testers, don’t know Y and mitochondrial DNA testing for genetic genealogy exists, or how it can help their genealogy research, which is extremely ironic since these were the first tests available, back in 2000.

You can read about finding Y and mitochondrial information for various family lines and ancestors and how to assemble a DNA Pedigree Chart here.

You can also take a look at my 52 Ancestors series, where I write about an ancestor every week. Each article includes some aspect of DNA testing and knowledge gained by a test or tests, DNA tool, or comparison. The DNA aspect of these articles focuses on how to use DNA as a tool to discover more about your ancestors.

 

Testing for Medical/Health or Traits

The DTC market also includes health and medical testing, although it’s not nearly as popular as genetic genealogy.

Health/medical testing is offered by 23andMe, who also offers autosomal DNA testing for genealogy.

Some people do want to know if they have genetic predispositions to medical conditions, and some do not. Some want to know if they have certain traits that aren’t genealogically relevant, but might be interesting – such as whether they carry the Warrior gene or if they have an alcohol flush reaction.

23andMe was the first company to dip their toes into the water of Direct to Consumer medical information, although they called it “health,” not medicine, at that time. Regardless of the terminology, information regarding Parkinson’s and Alzheimer’s, for example, were provided for customers. 23andMe attempted to take the raw data and provide the consumer with something approaching a middle of the road analysis, because sometimes the actual studies provide conflicting information that might not be readily understood by consumers.

The FDA took issue with 23andMe back in November of 2013 when they ordered 23andMe to discontinue the “health” aspect of their testing after 23andMe ignored several deadlines. In October 2015, 23andMe obtained permission to provide customers with some information, such as carrier status, for 36 genetic disorders.

Since that time, 23andMe has divided their product into two separate tests, with two separate prices. The genealogy only test called Ancestry Service can be purchased separately for $99, or the combined Health + Ancestry Service for $199.

If you are interested in seeing what the Health + Ancestry test provides, you can click here to view additional information.

However, there is a much easier and less expensive solution.

If you have taken the autosomal test from 23andMe, Ancestry or Family Tree DNA, you can download your raw data file from the vendor and upload to Promethease to obtain a much more in-depth report than is provided by 23andMe, and much less expensively – just $5.

I reviewed the Promethease service here. I found the Promethease reports to be very informative and I like the fact that they provide information, both positive and negative for each SNP (DNA location) reported. Promethease avoids FDA problems by not providing any interpretation or analysis, simply the data and references extracted from SNPedia for you to review.

I would be remiss if I didn’t mention that you should be sure you really want to know before you delve into medical testing. Some mutations are simply indications that you could develop a condition that you will never develop or that is not serious. Other mutations are not so benign. Promethease provides this candid page before you upload your data.

Different files from different vendors provide different results at Promethease, because those vendors test different SNP locations in your DNA. At the Promethease webpage, you can view examples.

Traits

Traits fall someplace between genealogy and health. When you take the Health + Ancestry test at 23andMe, you do receive information about various traits, as follows:

Of course, you’ll probably already know if you have several of these traits by just taking a look in the mirror, or in the case of male back hair, by asking your wife.

At Family Tree DNA, existing customers can order tests for Factoids (by clicking on the upgrade button), noted as curiosity tests for gene variants.

Family Tree DNA provides what I feel is a great summary and explanation of what the Factoids are testing on their order page:

“Factoids” are based on studies – some of which may be controversial – and results are not intended to diagnose disease or medical conditions, and do not serve the purpose of medical advice. They are offered exclusively for curiosity purposes, i.e. to see how your result compared with what the scientific papers say. Other genetic and environmental variables may also impact these same physiological characteristics. They are merely a conversational piece, or a “cocktail party” test, as we like to call it.”

Test Price Description
Alcohol Flush Reaction $19 A condition in which the body cannot break down ingested alcohol completely. Flushing, after consuming one or two alcoholic beverages, includes a range of symptoms: nausea, headaches, light-headedness, an increased pulse, occasional extreme drowsiness, and occasional skin swelling and itchiness. These unpleasant side effects often prevent further drinking that may lead to further inebriation, but the symptoms can lead to mistaken assumption that the people affected are more easily inebriated than others.
Avoidance of Errors $29 We are often angry at ourselves because we are unable to learn from certain experiences. Numerous times we have made the wrong decision and its consequences were unfavorable. But the cause does not lie only in our thinking. A mutation in a specific gene can also be responsible, because it can cause a smaller number of dopamine receptors. They are responsible for remembering our wrong choices, which in turn enables us to make better decisions when we encounter a similar situation.
Back Pain $39 Lumbar disc disease is the drying out of the spongy interior matrix of an intervertebral disc in the spine. Many physicians and patients use the term lumbar disc disease to encompass several different causes of back pain or sciatica. A study of Asian patients with lumbar disc disease showed that a mutation in the CILP gene increases the risk of back pain.
Bitter Taste Perception $29 There are several genes that are responsible for bitter taste perception – we test 3 of them. Different variations of this gene affect ability to detect bitter compounds. About 25% of people lack ability to detect these compounds due to gene mutations. Are you like them? Maybe you don’t like broccoli, because it tastes too bitter?
Caffeine Metabolism $19 According to the results of a case-control study reported in the March 8, 2006 issue of JAMA, coffee is the most widely consumed stimulant in the world, and caffeine consumption has been associated with increased risk for non-fatal myocardial infarction. Caffeine is primarily metabolized by the cytochrome P450 1A2 in the liver, accounting for 95% of metabolism. Carriers of the gene variant *1F allele are slow caffeine metabolizers, whereas individuals homozygous for the *1A/*1A genotype are rapid caffeine metabolizers.
Earwax Type $19 Whether your earwax is wet or dry is determined by a mutation in a single gene, which scientists have discovered. Wet earwax is believed to have uses in insect trapping, self-cleaning and prevention of dryness in the external auditory canal of the ear. It also produces an odor and causes sweating, which may play a role as a pheromone.
Freckling $19 Freckles can be found on anyone no matter what the background. However, having freckles is genetic and is related to the presence of the dominant melanocortin-1 receptor MC1R gene variant.
Longevity $49 Researchers at Harvard Medical School and UC Davis have discovered a few genes that extend lifespan, suggesting that the whole family of SIR2 genes is involved in controlling lifespan. The findings were reported July 28, 2005 in the advance online edition of Science.
Male Pattern Baldness $19 Researchers at McGill University, King’s College London and GlaxoSmithKline Inc. have identified two genetic variants in Caucasians that together produce an astounding sevenfold increase of the risk of male pattern baldness. Their results were published in the October 12, 2008 issue of the Journal of Nature Genetics.
Monoamine Oxidase A (Warrior Gene) $49.50 The Warrior Gene is a variant of the gene MAO-A on the X chromosome. Recent studies have linked the Warrior Gene to increased risk-taking and aggressive behavior. Whether in sports, business, or other activities, scientists found that individuals with the Warrior Gene variant were more likely to be combative than those with the normal MAO-A gene. However, human behavior is complex and influenced by many factors, including genetics and our environment. Individuals with the Warrior Gene are not necessarily more aggressive, but according to scientific studies, are more likely to be aggressive than those without the Warrior Gene variant. This test is available for both men and women, however, there is limited research about the Warrior Gene variant amongst females. Additional details about the Warrior Gene genetic variant of MAO-A can be found in Sabol et al, 1998.
Muscle Performance $29 A team of researchers, led by scientists at Dartmouth Medical School and Dartmouth College, have identified and tested a gene that dramatically alters both muscle metabolism and performance. The researchers say that this finding could someday lead to treatment of muscle diseases, including helping the elderly who suffer from muscle deterioration and improving muscle performance in endurance athletes.
Nicotine Dependence $19 In 2008, University of Virginia Health System researchers have identified a gene associated with nicotine dependence in both Europeans and African Americans.

Many people are interested in the Warrior Gene, which I wrote about here.

At Promethease, traits are simply included with the rest of the conditions known to be associated with certain SNPs, such as baldness, for example, but I haven’t done a comparison to see which traits are included.

 

Additional Vendor Information to Consider

Before making your final decision about which test or tests to purchase, there are a few additional factors you may want to consider.

As mentioned before, Ancestry requires a subscription in addition tot he cost of the DNA test for the DNA test to be fully functional.

One of the biggest issues, in my opinion, is that both 23andMe and Ancestry sell customer’s anonymized DNA information to unknown others. Every customer authorizes the sale of their information when they purchase or activate a kit – even though very few people actually take the time to read the Terms and Conditions, Privacy statements and Security documents, including any and all links. This means most people don’t realize they are authorizing the sale of their DNA.

At both 23andMe and Ancestry, you can ALSO opt in for additional non-anonymized research or sale of your DNA, which you can later opt out of. However, you cannot opt out of the lower level sale of your anonymized DNA without removing your results from the data base and asking for your sample to be destroyed. They do tell you this, but it’s very buried in the fine print at both companies. You can read more here.

Family Tree DNA does not sell your DNA or information.

All vendors can change their terms and conditions at any time. Consumers should always thoroughly read the terms and conditions including anything having to do with privacy for any product they purchase, but especially as it relates to DNA testing.

Family Tree DNA archives your DNA for later testing, which has proven extremely beneficial when a family member has passed away and a new test is subsequently introduced or the family wants to upgrade a current test.  Had my mother’s DNA not been archived at Family Tree DNA, I would not have Family Finder results for her today – something I thank Mother and Family Tree DNA for every single day.

Family Tree DNA also accepts transfer files from 23andMe, Ancestry and very shortly, MyHeritage – although some versions work better than others. For details on which companies accept which file versions, from which vendors, and why, please read Autosomal DNA Transfers – Which Companies Accept Which Tests?

If you tested on a compatible version of the 23andMe Test (V3 between December 2010 and November 2013) or the Ancestry V1 (before May 2016) you may want to transfer your raw data file to Family Tree DNA for free and pay only $19 for full functionality, as opposed to taking the Family Finder test. Family Tree DNA does accept later versions of files from 23andMe and Ancestry, but you will receive more matches if you test on the same chip platform that Family Tree DNA utilizes instead of doing a transfer.

Additional Vendor Considerations Summary Chart

Family Tree DNA Ancestry 23andMe
Subscription required in addition to cost of DNA test No Yes for full functionality, partial functionality is included without subscription, minimum subscription is $59 by calling Ancestry No
Customer Support Good and available Available, nice but often not knowledgeable about DNA Poor
Sells customer DNA information No Yes Yes
DNA raw data file available to download Yes Yes Yes
DNA matches file available to download including match info and chromosome match locations Yes No Yes
Customers genealogically focused Yes Yes Many No
Accepts DNA raw data transfer files from other companies Yes, most, see article for specifics No No
DNA archived for later testing Yes, 25 years No No
Beneficiary provision available Yes No No

 

Which Test is Best For You?

I hope you now know the answer as to which DNA test is best for you – or maybe it’s multiple tests for you and other family members too!

DNA testing holds so much promise for genealogy. I hesitate to call DNA testing a miracle tool, but it often is when there are no records. DNA testing works best in conjunction with traditional genealogical research.

There are a lot of tests and options.  The more tests you take, the more people you match. Some people test at multiple vendors or upload their DNA to third party sites like GedMatch, but most don’t. In order to make sure you reach those matches, which may be the match you desperately need, you’ll have to test at the vendor where they tested. Otherwise, they are lost to you. That means, of course, that eventually, if you’re a serious genealogist, you’ll be testing at all 3 vendors.  Don’t forget about Y and mitochondrial tests at Family Tree DNA.

Recruit family members to test and reach out to your matches.  The more you share and learn – the more is revealed about your ancestors. You are, after all, the unique individual that resulted from the combination of all of them!

My Son in Vietnam – The Story of Bob and Nahn

Have you ever seen a “birth” announcement for a 48 year old child’s arrival? No? Well, you have now.

nhan-birth

Meet Nahn, son of Bob Thedford. You see, Bob never knew that Nahn existed, and Nahn didn’t know how to find his father.

For 48 years, Nahn dreamed and Bob had no idea…and then one day…that all changed, thanks to a DNA test at Family Tree DNA.

I became peripherally involved in Bob and Nahn’s story in 2013 when Bob’s wife, Louise, contacted me, in shock.

Bob, Nahn and Louise’s story is a bittersweet mix of sorrow and joy. I want to let Louise tell the story. After Nahn’s discovery, Louise created a document chronicling what happened so she didn’t have to write the same information over and over again to various people who wanted to know “what happened.”

Bob’s DNA Story

I want to relate a DNA story that happen in our family that added an unexpected branch to our family tree.

I took my first mtDNA test with Family Tree DNA in early 2006 and received my mitochondrial results in June 2006. In July 2010, I received results from a Family Finder DNA test. Then in March of 2012, I received results mt Full Sequence test.

When I was ordering my mt Full Sequence upgrade, I mentioned to my husband what I was doing. He said, “I want to take a DNA test. Can you order me a kit?”  So I placed an order for him for a Family Finder kit. We both received our results in March of 2012. At that time we had no idea of the life changing experience that was in store for us.

A few months later I ordered a kit for my son, our daughter and Bob’s mother. It was worked out between all of us that I would be the administrator of all kits. Checking on matches, following up on e-mails, contacting matchings. Anything that needed to be done to connect with distant cousins.

In September of 2013 we discovered that my husband had a Skin Cancer. It was caught in the early stages and we had hope that with proper treatment he could be cured.

Toward the end of September 2013, I went on-line to check all the FTDNA profiles for new matches. I have to login into each profile one at a time.

I would always check my profile first. On this night I has a few new matches but nothing that really caught my eye at the time.

Next I logged into my husband’s profile. He had a new match near the top of his match list just under our daughter and his mother.  I sat there and stared at the screen for a couple of minutes trying to comprehend what I was seeing.

The name on the screen was one I had never heard in the past. But the shared centiMorgans between my husband and this person was in the parent / child relationship range.

Our daughter shared 3,380 centiMorgans with her father. And this person shared 3,384 centiMorgans with my husband. I kept staring at the screen and the thought that was running through my head, the lab has made a mistake!!

nhan-match

I decided to contact Roberta Estes who writes a DNA Blog.  I explained to Roberta my findings. I said, “I think I already know the answer, but could there be a mistake by FTDNA in interpreting Vo Hun Nhan’s results?”

Her reply to me was, “I have never seen the lab make a mistake of the kind it would take for this to be in error.  Having said that doesn’t mean it couldn’t happen, but the entire process is automated via the tag on the vials.  I can’t even imagine how it would happen.”

I had checked our daughter and my mother-in-law’s profile, finding the same name with large amounts of matching centiMorgans. I began to think that the lab had not made a mistake.

After lot of investigation and e-mails to several people, we confirmed that Vo Huu Nhan is my husband’s 48 year old biological son. Without the DNA test we would never know of his existence. My husband had no idea that he had a son.

On October, 15, 2013, Bob reached out to Nahn’s contact, asking how to contact Nahn. Bob served in the Vietnam War from March 1968 to March 1969. Nhan was born in August 1969.

After my husband returned to the States he had 8 months left on his tour of duty. He was sent to Redstone Arsenal, Huntsville, Alabama to finish out his tour. Huntsville is my home and that is where we first came to know each other.

Bob’s tour of duty was over in December 1969 and he returned back home to Fort Worth, Texas. It was not long after he returned back to Texas, that me and my 5 year old son moved to Fort Worth.

Four days after Bob reached out to Nahn’s contact, we received this letter about what Nahn said when he was told that they had found his father.

“I just received a message from Nhan’s best friend (Son Tran who introduced Nhan to me and asked me to give Nhan a chance to have a DNA test) that Nhan was very happy about the news… He said that “he would not be happier if someone gave him a million dollar than give him a father!!”

The results of the DNA test were bittersweet. All of the family was overly excited to have found Nhan but were sad to find out that for all these years we did not know of his existence. Nhan lives in South Vietnam in the Mekong Delta, he doesn’t speak English and does not own a computer.

All Nhan had been told about his father was that he was an American G.I. and his name was Bob. That was after he came home crying and asking his grandmother “Why the kid’s made fun of him and why did he look different compared to everyone else.” He looks more like Bob’s father than looks like Bob. Another thing we couldn’t deny after seeing a picture of him.

How Nhan came to know about the DNA test was through a childhood friend that lives in Ho Chi Minh City (Saigon). His friend Dang Van Son had heard that DNA kits were being brought to Saigon and that they were looking for “Children Left Behind” to come and take the test.

nhan-with-friend

Nahn and his friend, Son, in Vietnam. Son arranged for Nahn’s DNA test.

Son contacted Nhan and told him he should come and take the test. They only had 80 test kits to go around. I don’t know how many came for the test but Nhan was able to be tested.

After we confirmed that all was legit. Son began to e-mail us and send pictures of Nhan and his family as well as send messages from Nhan.  Nhan has 5 children, 1 son and 4 daughters.

nhan-with-children

Nahn has 3 grand-children by two daughters. This added 9 new family members to my Family Tree. Nhan has been married twice. One marriage ended in divorce and his second wife died of liver cancer about 2008.

Nhan had several jobs in Vietnam so I was told by his friend Son. Porter in market, rescue diver, worked on a floating market boat.

nhan-working

On Christmas morning of 2013 we received a call from Vietnam. It was Nhan calling to wish us a Merry Christmas. His friend Son’s daughter translated. Then we received an e-mail picture of the family. We were able to Skype with him one time before my husband passed away.

In 2014, Louise and Bob discovered how difficult Nahn’s life had been. Nahn’s friend, Son, sent them the following:

nhan-letter-2

You can learn about the lives of mixed American and Vietnamese children in this YouTube video, along with information about Trista Goldberg who founded Operation Reunite and partnered with Family Tree DNA to reunite these families.

Louise continues:

On April 17, 2015 before Bob passed away a few days later on April 26, the Washington Post published an article “Legacies of War” Forty years after the fall of Saigon, soldiers’ children are still left behind. They profiled 5 children still looking for their father’s. The lead story was about my husband and Nhan.

There is a picture in the article where they are sitting in front of the computer. The reporter is Skyping with our daughter Amanda for the story. That is Amanda on the screen. The second story is about Nhan’s childhood friend Dang Van Son that has been such a help to us and Nhan with keeping us in touch with each other.

nhan-skyping

Amanda and Nahn Skyping.

On the day Bob passed away, our local paper, the Fort Worth Star Telegram’s front page story was the story about my husband and Nhan from the Washington Post, Legacies of war connect Vietnam, Tarrant County.

It was so surreal to be walking to the coffee shop and pass all the newspaper’s boxes and see Bob and Nhan’s picture in the window of the boxes. Bob was in hospice at the hospital and we knew it was a matter of time, and shortly he would not be with us anymore.

By the time these articles were published my husband was to the point of non-communication. The Washington Post had wanted to Skype with me and Bob but it was not possible. Bob passed away on Sunday night, April 26, 2015.

I knew that Bob was critically ill, then Louise informed me that Bob had passed away. I was just heartsick that Bob and Nhan never had the opportunity to meet in person. It seemed that a dream for both Bob and Nahn, so close, finally within reach, had just slipped away. I thought, at that time, that this was the end of the story, and certainly not the ending any of us wanted – but it wasn’t the end after all.

Twenty-one months later, I heard from Louise again, this time with very unexpected news.

A Visa for Nahn

Again, from Louise:

In October of 2015 we received an e-mail from Trista Goldburg the person with “Operation Reunite” who bought kits from Family Tree DNA and took them to Saigon for testing.

She had received an e-mail from Franc Shelton, Country Fraud Prevention Coordinator, Mission Vietnam FPU, U.S. Consulate General Ho Chi Minh City, Vietnam.

Dear Trista,

I hope you are well.  I would like to  encourage you to reach out to the family of Robert Thedford and urge the daughter of Mr. Thedford to consider undergoing another DNA collection, and to pay for a collection here at the consulate for Mr. Vo, at one of the approved labs from the list I sent you.

We just had a case in which we were able to close out because the parties involved proceeded in the manner which I discussed with you—in that case, the American father is practically indigent, but fortunately there were Viet Khieu benefactors in California who generously paid for the testing.  I moved that case to the front of the line and expedited all our procedures-we collected the alleged son’s sample here on 30 September and had the results back 2 weeks later (99.99%).  I hand-carried the results to the immigrant visa unit and strongly encouraged them to expedite their own processes (I have no control over that however).

Amanda was going to take a second test and we would pay for the test. The lab closest on the AABB Accredited Relationship (DNA) Testing Facilities list was, University of North Texas, Fort Worth, Texas.

When Amanda contacted them she was told they no longer did DNA testing. She replied back to Trista and let her know what she found. There were a few more letters exchanged. Amanda never did take a second test. We did not hear anything more for several months until July of this year when we received and e-mail from Nhan with a copy of his and his daughters Immigration Visa’s.

Nahn’s Letters

I have to share with you two letters Nhan sent to me. I feel sure his friend Son wrote the letter as Nhan dictated them. They are so sweet.

DEAR  MU USA  MUM,

ALLOW  ME  TO CALL    YOU  AS  MY USA  MUM.

IAM HAPPY THAT I HAVE  TWO  MUM  IN THE WORLD

  1. USA  MUM,
  2. VIETNAMSE MUM,

HAVE  GOOD MORNING MY USA MUM.

MAY GOD BLESS US

MY WARMEST REGARDS  TO YOU AND THE FAMILY,

STEP SON OF  LOVED HUSBAND  OF YOU.

VO HUU  NHAN.

1/JULY 2016 DEAR  MY USA MOTHER,

And another letter.

I DO  THANK  TO EVERY-ONE  WHO HELPED  ME  IN DNA  TESTING RESULLT,  AND BASING ON DNA TEST RESULT  I  KNOW  YOUR HUSBAND  IS  MY  BIOLOGCAL FATHER,

  DEAR  MY USA  MOTHER WITH YOUR  HELP  TODAY  I   WILL  OWN  FOR EVERYTHING YOU HAVE DONE  TO HELP ME,

I WILL  WORK  TO BE COME  AN US CITIZEN AS SOON AS I CAN,

I ALWAYS  AM  PROUD  OF MY US FATHER

I PRAY FOR HIM  DAILY   AND NOW HE HAS HIS LIFE  ON THE HEAVEN IT IS  THE BEST LIFE FOR HIS SOUL

AND I THINK HIS SOUL  ALWAYS  SHOW ME  THE WAY TO GO TO ——–

THANK   US MOTHER!

APPLICANT: VO HUU  NHAN

 11/JULY/2016

A Christmas Surprise

As these events unfolded, I was pulling for Louise and Bob, and rooting for Nahn, but without understanding the immigration process, there was little I could do to help. In fact, I didn’t think there was much anyone could do to help Nahn.

When Louise’s update e-mail arrived a few days after Christmas in 2016, it was with pictures – of Nahn – here – with her in the US. I was amazed, to put it mildly. A miracle had happened.

nhan-with-louise

Nahn and his American Mom, Louise

Not only that, but Nahn arrived with his mother and his youngest daughter – and not just to visit, but to live in the US permanently.

nhan-mother-daughter

Nahn, his Vietnamese mother and daughter in Texas, a few days after arrival, visiting Louise.

I asked Louise how Nahn’s arrival felt, for her and Amanda, given that Bob was gone and had so much wanted to meet Nahn. In a very real way, they were living Bob’s dream for him.

Yes it was a bittersweet reunion without Bob being here to enjoy it with us. Our daughter, Amanda, was excited about the meeting. She is my and Bob’s only child and now she has two half brothers.

nhan-with-amanda

Nahn and Amanda, half-siblings, meeting for the first time in Texas.  I love their smiles.  They look so happy!

Amanda has lived such a different life than Nhan. Nothing extravagant, her father has a hard-working police officer and worked a second part time job for 23 years to allow me to stay home with Amanda. Amanda earned her own way through college, but had so many more opportunities than Nahn. It’s so sad that Bob never knew Nahn existed.

Nhan has been able to prove he has an American father. Nhan, his youngest daughter, 12 year’s old, and his mother have been granted immigration visa’s. Nhan, his mother and daughter arrived at Dallas-Fort Worth International Airport on Tuesday night December 20th, 2016, thirty-six hours after leaving Vietnam.

I thought that Nahn and his family came for a visit, but that’s not the case, according to Louise.

My understanding is that Nhan, his mother and daughter plan to make Texas their new home. Currently they are living in Dallas, which is an hour or so from where I live. I am in contact with their Refugee Resettlement Case Worker at Refugee Services of Texas.

The case worker told me the night they arrived it was very cold, they came with one small bag of clothes and the clothes they had on. Clearly they weren’t prepared for winter. The next day, helping them settle in, she took them to a Walmart and said they walked in and their eyes got big and they said “WOW”!!!!!!!!!

Their case worker said her next goal is to help Nahn find a job. She will also help him learn how to ride a bus for transportation.

Nahn and his family have so many obstacles to overcome living here. The major one is the language barrier. None of them know any English except “Thank You, Hello” and “WOW” although they are already taking English classes.

nhan-with-daughter

Nahn and his daughter – their first Christmas in Texas, a few days after arrival.

In many ways, Nahn, his mother and daughter represent the journey of so many of our ancestors who arrived with the hope of making better lives for themselves and their children. They too arrived without knowing the language and with few, if any, belongings. The difference is that they often arrived in a group of other immigrants from the same country – so they had extended family and help – and others who could speak the language. Nahn and his small family arrived in a group of just 3.

I can only think how difficult the life they left must have been to warrant this kind of foray, really a leap of incredible faith, into an totally unknown world where an entirely uncertain future is more attractive than one’s current life. Nahn, his mother and daughter are incredibly brave. At some level, they must certainly be unspeakably frightened too.

I would be terrified, wondering how I would eat, how I would live, where I would live and would I be able to find work to provide for myself, my mother and a daughter with special needs.

One thing is for sure, Bob would be busting-the-buttons-off-his-shirt proud of Nhan.

How to Help

Knowing my blog readers, I know your next question will be how you can help Nahn and his family. I’m not sure what they will need from day to day, and what has already been taken care of. Please feel free to contact Nhan’s case worker, below, if you know of a job or want to help in another way.

Kate Beamon at Refugee Services of Texas
9696 Skillman, Suite 320 Dallas, TX 75243

Phone, (214) 821-4883
e-mail, kbeamon@rstx.org
http://www.rstx.org/about-us.html

Acknowledgements

A heartfelt thank you to Louise for sharing this very personal story of her family’s journey.

Louise conveys a special thank you from her family to Bennett Greenspan at Family Tree DNA.

Looking for and Contacting Birth Family Members

When I ran the article title DNA Testing Strategy for Adoptees and People with Uncertain Parentage, one commenter asked how one goes about putting together the pieces of the puzzle, and then how does one go about making contact?  What do you do, or say, to increase your likelihood of being successful?

I am probably the all-time worst person to answer this question, because I intensely dislike telephone conversations and especially in awkward situations.  My family has had a few of those awkward parentage situations, mostly having to do with my father and grandfather, both “ladies men,” and I’ve been both rejected and hung up on more than once – so you don’t want advice from me on this topic.

I turned to someone with a track record of success – not only in terms of putting together the convincing evidence about the missing parent – but in terms of preparation for contact, approach and actually making the contact.

Diane Harman-Hoog, with www.dnaadoption.com was kind enough to write this article.

DNAadoption page

Diane works with adoptees and others seeking their biological parents every day.  She is a retired technology professional, so transitioning her skills to a genetic genealogy puzzle was the perfect fit for Diane.  In addition to working with a team who has developed the specific search techniques, sometimes in spite of some of the vendors we have to work with, Diane has created an educational venue and teaches others the techniques and how to help themselves.

Diane is summing up a significant process here, in just a few paragraphs.  If you’d like to know more about these techniques, please visit http://www.dnaadoption.com and take a look at their class offerings.

Many people call Diane and the people at DNAAdoption search angels – that’s because they truly are.  Not only are they reuniting families, when the family wants to be reunited – but Diane and her team are providing the adoptee with a history, something they have never had.  Thank you so much Diane – for this article and for everything that you and the folks at DNAadoption do.

From Diane Harman-Hoog

We at DNAadoption are having a great deal of success with reuniting birth family members with adoptees and with others who have lost track of a father, for example.

One of the first things an adoptee should do is try to get their non-identifying birth information, if available, through their adoption agency.  Many times this alone can be used in a traditional search even without DNA.  If they have non-id that is older than 5 years, we recommend they apply for an update. We at www.DNAAdoption.com can help if they don’t know how to go about this process.

The DNA Search Process

The world was a lot easier before Ancestry decided to ignore what we all felt were hard and fast principles of the search – meaning providing the tester with chromosome match information – the chromosome number and start and stop locations of matching DNA. We collected chromosome data and “In Common With” genealogy data, ran them through our programs with resulting spreadsheets that group overlapping DNA into sets and then noted which people in that set were ICW with others in the set.

A definition or two is in order here. I prefer to tell students that ICW means blood related. Overlapping means any part of the chromosome segments that overlap, they do not have to be the same length.

Identification by Triangulation

We can have two people with starting and ending addresses on a particular chromosome which makes us think that they received the segment from the same ancestor. However, nature plays a little joke with us on that part, because there are two sides to the chromosome and each side has the same address sequence. On one side, the addresses increase going one way and on the other side, they increase going the other way.

When we identify people who look like they have overlapping chromosomes then if they are blood related with each other, then the segments came from the same ancestor. The very small segments are probably not indicative of family heredity but are environmentally caused genetic strings.

I use this example of blood related. You are blood related (ICW) with all your matches as you are the very bottom of the relationships and related to both sides. You maternal grandmother is probably not blood related or ICW with your paternal grandfather. In most cases, they come from different families.

In general, the longer the segment the closer the relationship, but when the prediction is closer than second cousins, we start to look at the total of all the segments over about 6 cM (centimorgans) that overlap.

Then we look for common ancestors using the trees of those two individuals. Next is triangulation where three people match on the same segment. That is because every one of your matches overlaps with your DNA segments and is always ICW with you. So two plus one gives us the three to triangulate.

In order to look for common ancestors on the trees, you need 3 things:

    • Overlapping DNA segments
    • ICW status between the same individuals
    • And some tree information from each party.

Expanding trees

We get as much of the tree that we can for each person and then we have to go to work expanding the existing tree. First the tree must go up in the traditional genealogical manner, you, your parents, your grandparents etc. You also treat any matching person the same way so you get a normal looking genealogical tree. If this is a 2nd cousin match, take the tree back to at least 3 generations past the great grandparents.

Then comes the really tedious part. You come back down the tree identifying all the offspring and all of their offspring down to the years where you would expect the grandparent or other unidentified person to be living. As you go down the tree (towards the present), you must also add each spouse for each of the offspring and go up their ancestry a ways to see if they might also be related. By the time you get down to the actual candidate of the father, you would hope to find that both his mother and father are related to DNA matches of yours.

The difficulty often comes from two directions, incomplete trees that you just cannot fill in and completing the most recent generations. At that point we have to rely on Google searches and obituaries to make the final identifications.

In essence, the DNA identifies who you are related to, triangulation identifies groups of people who share a common ancestor, and their trees will lead you to the identification of both that common ancestor and hopefully, your parent.

If this is a little sketchy, the full course takes 4 weeks and I am trying to summarize it here. Some searches only take a tree or two but I have also done ones that took 200 trees (and five years).

Ancestry

Then Ancestry came along and is refusing to give us the chromosome numbers. This is particularly bad for adoptees who rely upon those numbers to confirm or deny the relationships.

So we deal with it in this manner. We have a DNA software Client for ancestry called DNAGedcom from the DNAGedcom site. It reads your Ancestry DNA account and generates a match list of all your matches and an ancestors list of all the ancestors of those matches. A more recent addition is also an ICW list to show us which matches are ICW with which other matches.

Gedmatch

Whenever possible do everything you can to encourage these matches to download onto Gedmatch.

Another trick, after you transfer the kits to Gedmatch, is to use the report on Gedmatch, named “People who match one or both of 2 kits”. This report takes the gedmatch # of two individuals and measures them against each other. If I run it against my brother, Ken, and my maternal cousin, Jon, I will get three different lists. The first list is of kits that both Jon and Ken match. Since our mother and Jon’s mother are sisters, then we can assume that these are maternal matches for both Jon and Ken. The second list shows kits that only Jon matches, that would be from his father’s side of the family and the third list shows only kits that Ken matches so that would be cousins that Ken matches who are not maternal but from our father’s side.

It must be understood that using DNA analysis is not an exact science but a learned art as DNA inheritance can be capricious. We are working with probabilities and averages here. We cannot say that there are 169 cM of DNA shared, so the match is a second cousin, but rather, the match might be a second cousin.

Now we play the odds. We match ancestors from the ancestors list and as a start call them Common Ancestors.  So if both Ancestry trees have Pierre LeBlanc born in 1769  in Louisiana and both Pierre’s have the same parents we call them common ancestors until proven otherwise. The odds are actually fairly high if the two families are ICW with each other.

We cannot just say that a child of Pierre LeBlanc is absolutely in Jon’s direct line but we will expand the trees and trace individuals down. If they eventually start lining up with other DNA match descendants we will accept that it is direct line. However, of course NPEs are always a concern and there is no way to completely protect from that eventuality.

phone

Contact Time

As you continue the search now, with live people, do not use the word “adoption” until you are certain of the relationship with the person you are speaking to. This includes people like a librarian, as well as possible relatives. Some people feel strongly about not assisting adoptees in finding a birth family. One of my clients let it slip to a first cousin. That was the end of the relationship. We really needed information that cousin had.

So now we have built trees down and have three males who were in the correct vicinity at the correct time for conception. Each of these males has one line descending from a DNA match, but only one has the other parent also descending from a DNA match!

Our tree has developed to include possible common ancestors from all three tests and gedmatch.

We try to obtain up-to-date contact information which in these days of cell phones is harder to get than it used to be.

The only person we encourage to make contact is the adoptee or another birth family member who is looking. None of us will do it for them. If contact is refused then at least they have talked to the person once.

Whether we are down to the exact level or perhaps only to a cousin or aunt or uncle, we advise proceeding with caution. We advise the contact to be made on the basis of DNA information and asking for help with a family tree. A lot of detective work goes on before a phone call is made to confirm the suspicions – at least as much as possible. We check where people were at that time, or did a woman have a child born at a time that would mean that this child could not have been hers. What was their life like?  Do most facts line up with the non-ID information? It is possible that the non-ID is fictional but we assume that most of it is right until we prove otherwise.

Making the Call

If a man is calling the person we are pretty sure is his birth mother, the conversation will go something like this. ”I am looking to fill in some members of my family tree and DNA testing shows that we might be related. I am quite sure I am related to the Woolworth line from talking to other matches. I want to be sure you have my contact information in case you think of something that might help me after we talk, email is –, my phone number is –. I was born on October 1, 1963 in Syracuse NY. Does that mean anything to you?  (Hoping for a positive indication.) Yes I was adopted, My adoption papers are hard to read, but my birth name might have been Dennis. The state has given me a little information about my birth mother, she was 26 and in secretarial school. Her mother was 56 and her father deceased. She had a sister and two brothers.”

Hopefully by then she is in tears.  Most birth mothers have been praying to be found. If she is unhappy then he should give her some time. He has provided contact information for himself. Also he should send her a little card afterward, thanking her for her time and provide a picture of himself and his family, along with his contact information.

Good luck to you all.

Diane Harman-Hoog

You can contact Diane at harmanhoog@gmail.com

How They Found the Real Benjamin Kyle

Benjamin Kyle 2010

The genetic genealogy community let out a simultaneous whoop for joy last week at the news that the identity of Benjamin Kyle had finally been found. At long last, the “man with no name” finally has a name – a real name – not a temporary name.

In case you’re not familiar, the man known as Benjamin Kyle was found beaten, stripped naked and left for dead behind a trash dumpster in 2004 in Richmond Hill, Georgia, outside Savannah.  He remembered nothing….nothing at all.  Not how he got there, not what happened, and not who he was.  His life became a living hell, because you not only can’t work, you can’t get any services, not even a bed in a homeless shelter, without being able to prove you are.  Surprised?  So was I.

Benjamin did remember snippets from time to time.  He remembered what he believed to be his birthday, 10 years to the day before Michael Jackson, and he remembered that he was Catholic.  He remembered landmarks in Indianapolis, Indiana as a child and some things from Colorado, but not much more.  He thought his first name might be Benjamin.

In 2008 Benjamin Kyle appeared on the Dr. Phil show, and in 2011, a documentary was produced about his plight.  Through this and other media coverage, his situation became known in the genetic genealogy community.  DNA testing commenced thanks to Family Tree DNA, and this saga culminated last week with the announcement that Benjamin’s identity has been found…along with his family…and yes…in Indiana.

Who accomplished this feat?  It wasn’t the police, as one might expect.  In fact, it is a little known group of “search angels” with www.DNAadoption.com, a nonprofit group that helps adoptees and others with unknown parentage find their roots through a combination of DNA testing and assembling the family trees of those whom they match, narrowing the search for their own family.  It’s a long tedious process, but it’s doable, and the DNAadoption volunteers developed and documented the methodology for success.

But hey, let’s listen as Diane Harman-Hoog tell this story herself in her article, Our Greatest Challenge.  After all, it’s their story, their victory – Diane along with the other search angels, and of course a victory for Benjamin Kyle too.  And for the inquiring minds who want to know exactly how the researchers accomplished this incredible feat….Diane shares the methodology!

Congratulations to all of the researchers and genetic genealogists involved in the search and discovery of the true identity of Benjamin Kyle.  I must say, in all of the footage I’ve seen of Benjamin, the video in the news article announcing the discovery of his identity is the first time I’ve ever seen him smiling and he looks genuinely happy!  It must have been an incredible day for Benjamin – like a second birth in one lifetime.  The gift of his life returned.

The folks at www.dnaadoption.com truly are angels.  Amazingly skilled, dedicated, devoted angels.  I’m positive that Benjamin Kyle would agree.  I do believe in the process of finding his original family that he has found a new family of genealogists too!

angel family

“Where do I come from?”

This is a true story, one of inspiration and hope, especially for adoptees or those seeking the identity of a parent.

I’ve been honored to be allowed to be a bystander, sometimes a coach, and often a cheerleader for my friend Mark…who…by the way, appears to be a distant cousin…although we don’t have the details figured out.  You know how us southerners are…we’re kin to everyone…as Mark is discovering.

After returning from the amazing experience of meeting his birth family members for the first time, he shared the latest chapter in his journey with me…and I’ve asked him to share it with you.  It’s beautiful and wonderful and let’s face it…finding family is the holy grail for us seekers.

Let me introduce you to guest author Mark and he’ll be telling you his story from this point on in his own words.

Mark

“Where do I come from?”

It’s a question everyone engaged in genealogy asks, but for those of us who are adoptees it has much more meaning.

I never asked my parents the question, although they had told me at a very early age that I was adopted. When I was young it was, “Oh, okay, what’s for lunch?”

They were already in their forties when they adopted me at birth right out of the hospital in Miami, and they never had another child. I was it, and kind of spoiled as a result. They were devoted to me and I to them, so while curious of my origins as I grew older, I never broached the subject for fear it might cause anguish or at least concern. I never wanted them to think I saw them as anything less than my real parents. For they were, always have been and always will be. I miss them very much.

Mark2

Still, the question lingered. Who am I?  Where did I come from?

I remember asking my aunt, actually my mother’s first cousin who lived in New York. She said I was Irish, probably because I resembled some of her Irish neighbors in Far Rockaway.

As a kid, I thought I was German since I kind of looked German and always wound up playing the German in soldier games and while terrible at French in school, excelled at German – little did I know.

I did know my ethnic heritage was not that of my parents – I didn’t look like them at all. As a child, my born-in-Russia grandmother would parade me down the boardwalk to meet her old friends. “Dat’s your grandzohn?” they would exclaim in obvious incredulity.

Mark3

Heritage and Health

Later, as an adult after my parents had passed, I began reading about genetics and how some diseases are inherited to varying degrees. It made me again think of the question and wonder if I could obtain genetic information that would answer the basic heritage question and the health question without necessarily finding a birth family. I saw no need to meet or contact my birth mother and cause anguish there.

So when I heard about National Geographic’s Genographic Project, I ordered the test right away. This was 10 years ago – boy, how time flies!

I’m sure everyone has experienced the thrill of receiving their first DNA results – I sure did. It came in a nice little package with a Certificate of Y-chromosome DNA Testing, which I still have, showing my haplogroup, R1b, and twelve short tandem repeat results. I had no clue what it all meant, but included was a nice map of the world showing that I came from – (drum roll) – Europe. Duh, that didn’t take rocket science to figure out, but genetic genealogy, or rather population genetics was still in its infancy.

Bitten by the Bug

Of course I wanted more, to know what those numbers stood for and what else I could find out. I was bitten by the DNA test bug and haven’t stopped.

I uploaded the results to Family Tree DNA, the lab that processed the Genographic results, to obtain what they then called Recent Ethnic Origins. This showed my closest matches at 12 STRs by country. I had three exact matches!

I thought I had found the answer – I was Scottish!  And two of the three were named MacGregor; I was a MacGregor! I started going to Scottish Festivals and Highland Games; bought the tartan tie and everything.

Mark Macgregor

Then I found out that 12 STRs doesn’t really tell you anything, even exact matches – you need to test 25, 37, 67 and on and on. I upgraded my markers,  contacted the MacGregor project administrator and received his reply, “Sorry, your STRs don’t match the MacGregor haplotype”

I was devastated, especially after spending money on MacGregor tchotchkes. I guess old man MacGregor has his own haplotype and to be a MacGregor you had to match his. So I tested at 25 and 37 and later at 67. No exact or even close matches at all – the MacGregors disappeared. I was left again without heritage.

I took more tests – Deep Clade and later Big Y for the Y-DNA and the full sequence for mtDNA. I now was R1b1b2a1b with a terminal SNP of L147.3, and H1ad on mtDNA, again simply European.

I shared a terminal Y-SNP with only one other gentleman. We were able to contact each other through the L176.2/SRY2627 project administrator and compare notes. Our STRs were not even close; he had estimated our MRCA at 500-1000 AD. He had traced his own paternal line to Northern Ireland and the Ulster Plantation, and probably back from there to the Borders area of England/Scotland. My Y-DNA could have come from anywhere in Western Europe.

Family Finder

I took the Family Finder test and again it showed European, western European with the largest percentage Orcadian

What the heck was Orcadian? Of course I had to look it up – people from the Orkneys. Well, we’re getting closer but how could they be that precise? It’s a tiny group of islands with a small population? Come to find out that FTDNA used data from the Human Genome Diversity Project that had as its only sample from the British Isles a handful of DNA tests from the Orkneys. Not much precision there! My DNA was simply closer to people from the Orkneys than say Upper Sandusky.

I also received, as one does with Family Finder, a list of cousin matches. Now we’re getting somewhere, as I have to date 102 pages of matches, 7 pages at the 2nd to 4th cousin range. I thought I might find a pattern, like a group of those closest with the same surname, say MacGregor (out of spite).

But no, the names didn’t follow any pattern; my closest match had a German name but those following were not German. A few were even French-sounding; the horror!

My closest match emailed me to inquire about my pedigree. As I had done previously with a MacGregor match who had contacted me from Australia of all places, my response was that as an adoptee I had no information on my birth family, and unless they were aware of a female family member placing her newborn for adoption in Miami in 1952, I would not be of any help, sorry.

23andMe

I also tested with 23andMe and found their most recent Ancestry Origins test to be the most informative. I was still 99.3% European, but the breakdown had more detail and the sampling was of better quality. It even showed I had 1/2 of 1% Native American; now that’s interesting!

23andMe’s DNA Relatives lists 922 pages of cousin matches, many, including my four closest, without names or contact information, except the ability to send an introduction. Again of course there was no pattern.

The fifth closest match, a 3rd to 5th cousin, contacted me with the usual question. We exchanged emails but she couldn’t figure out how we related. My four closest matches never responded to an introduction.

But now at least I had some genetic health information. (This was before the FDA took that off market.) It was fascinating, how I had a .045 increased risk of this and .128 reduced risk of that. Nothing truly frightening, thank heavens.

Non-Identifying Information for Adoptees

Around this time, I became aware that the State of Florida made available “non-identifying information” for adoptees. This was perfect! I wasn’t looking to identify my birth mother, but to determine my heritage and any hereditary health issues. So I requested what they could provide, knowing that adoption records are otherwise sealed and unavailable except in medical emergencies.

A few weeks later I received a 2-page letter from the Florida Adoption Reunion Registry. This was in December 2010. It provided exactly what I was looking for, and much more. It said that my birth mother was born in the summer of 1920 in a Southern state, so she’d be over 90 at that time, if alive.

It described her features and that she worked as a waitress. It stated that she had come to Miami to live with her mother when she discovered her pregnancy, and that her mother was 52 at the time of my birth; so that her mother was born around 1900.

She reported that both her mother and father were Protestant and of Irish descent, that her father had died in 1929 and at the time was separated from her mother.

She also reported that she had two brothers, one with children and had had a sister who passed away. She said that her mother remarried and was separated from her second husband, and that her father, my birth grandfather, had been a farmer of English and Irish descent.

This was what I was looking for and more closely matched with my DNA results. I concluded she was describing a Scots-Irish heritage when she mentioned both Protestant and Irish together.

She also described my putative birth father, which came as much more of a surprise, if accurate. He was allegedly French Canadian! So much for the German in me. She said she had known him for only a short time, never intended on marrying him and never told him of her pregnancy. Most importantly, she said she did not know of any serious or communicable (sic) diseases in her family. I took that to mean hereditary diseases.

More Please

This was wonderful information, but it somehow left me wanting to know more. I’m sure as genealogists you all know the feeling.

What Southern state?

What was the background of her father’s parents?

Was there anything more on the birth father’s family?

I was resigned to the fact that this would remain a puzzle. After all, I was just seeking heritage, or was there more to my own feelings? I knew I wouldn’t try to contact my birth mother no matter how much information I had. The last thing I wanted was to give some 90-year old woman a heart attack. But that all remained academic anyway; there was not sufficient information to search for any birth family.

Until…

Ancestry.com

Last year I tested with Ancestry.com to compare what they would show on ethnic heritage with the two other companies.

It did not compare favorably; the percentages for different parts of Europe were way different from the others. It had 13% for Iberia while 23andMe had 2%, and 7% for Scandinavia while 23andMe had 1%. Maybe they realized that the Orkneys were settled by Vikings.

But what took me to the next level of answering “the question” was their Member Matches. At the top of the list was a 2nd cousin match, administered by the next closest match, also a 2nd cousin, her daughter Jeanene. And she had 955 people on her public family tree!

I couldn’t not look – the curiosity was overwhelming.

Besides, my birth mother had in all likelihood passed away by now and there was no perceived danger in contacting 2nd cousins. So I reviewed her family tree and found a possible candidate for birth grandmother, one Beulah Wooten, born in 1900, whose brother Levon was Jeanene’s grandfather. She and her mother would indeed be 2nd cousins if that were the connection. So I signed up for membership with Ancestry and began my own research.

Connecting the Dots to Beulah

I also decided to contact Jeanene.

She was happy to share what information she had on Beulah, including a recently found death certificate from 1957, listed as Beulah Wooten Ellis who had passed away at her home in Chattanooga, Tennessee. Intriguingly, the informant was listed as Mrs. Elizabeth Smith. The death certificate included her birth date of December 31, 1900.  It showed she was buried at Browns Gap Cemetery in Trenton, Georgia, just across the state line from Chattanooga.

I found the cemetery listed on Ancestry’s Find-a-Grave and found a gravestone showing both Beulah B. Langston with dates of birth and death matching that of the death certificate, and Eugene G. Langston, with a death date of March 16, 1928; very close to what the letter from the State had indicated.

I began to match up the facts reported in the non-identifying information provided by the State point-by-point with what I discovered in my research. It appeared Beulah married three times, the first to Eugene Langston who indeed turned out to be my birth grandfather, then to a Walter E. Jones with whom she had the two sons my birth mother reported as brothers, and finally to Alvis Ellis.

Beulah was listed with Alvis Ellis in the 1940 Census residing in Miami, Florida. Here was the connection to Miami.

Also buried at Browns Gap Cemetery was her daughter Junice Katherine Langston who was born in 1922 and died in 1937, matching my birth mother’s predeceased sister. While I could not find any birth certificates, one of those types of records Ancestry has so little of, I did find Beulah listed in the 1930 Census living in Chattanooga with her second husband Walter E. Jones, their two sons, and two daughters from her first marriage, Junice and Elizabeth Langston, age 10, and thus born around 1920. Was she the informant on the death certificate, born in 1920? This was the only reference I could find in my Beulah search to who I thought could possibly be my birth mother.

Suggestive, but not proof.

The Thrill of the Chase

Finding this information online was a thrill, and as you all know, one thing leads to another, requiring ever more research. I can easily see how genealogy can become an obsession. I see people on Ancestry who devote many hours a week over many years to it.

My hats off to those of you who have devoted decades before the internet driving from courthouse to courthouse, cemetery to cemetery, obtaining the information for your family trees.

I understand now, as I too have been bitten by the genealogy bug. That makes two bugs I’ve succumbed to.

I also see how some people make mistakes in their family trees, accepting others’ trees at face value without checking for themselves the sources for the information. My background as a retired attorney and former administrative judge leads me to require substantial evidence to support a fact and not simply accept what others have alleged. Which leads me back to Beulah and her daughter Elizabeth.

There was a private family tree on Ancestry that had an Elizabeth Langston listed. I contacted the person with the tree and mentioned the 1930 Census for the Jones household, asking if the Elizabeth Langston listed there was one and the same person. She replied that yes, it was, and was her husband’s grandmother, now deceased.

She stated, “Elizabeth had 3 children, two while married to Gilbert Conner, divorced (died 1955) Evelyn Conner Scott, Glenn Conner, (deceased) and Yvonne Smith while married to Almon Smith divorced (died1967). Married to William Lucas, lived and died in Portland Oregon, she passed away on Nov. 26, 2004. Hope this helps.”

It certainly did. The name Smith matched the informant on Beulah’s death certificate. I tried to contact her again, explaining who I was, but this time there was no response. I imagined my inquiry had caused quite a stir, or possibly she just ignored it fearing the stir it might cause, or perhaps thought I was misrepresenting myself and had other motives.

In any event, one Census report and one unconfirmed private family tree is not enough in my opinion to establish the fact of who my birth mother was. If true, then at least I knew she had passed away and the fear of her learning of the son she given up at birth 62 years before was gone. I still had to confirm her connection to Beulah, so my next step was to obtain a copy of the death certificate from Oregon.

Is Elizabeth Beulah’s Daughter?

You can imagine how anxious and excited I was opening the envelope containing Elizabeth’s death certificate.

That soon turned to joy.

There she was, born July 4, 1920, in Trenton, Georgia; occupation waitress; mother Beulah Langston. I had finished connecting the dots and matching up every fact from the non-identifying information the State of Florida provided with my research.

I had my proof – within a reasonable degree of certainty, as we say. There was still a deceased half-brother and two possibly living half-sisters out there, but my search for genetic heritage had led to finding my birth family, at least confirming Jeanene’s relationship as 2nd cousin through Beulah and her grandfather Levon.

There was simply no one else that matched up to Jeanene and her DNA.

More Than I Ever Expected

As I continued to research the Wooten and Langston lines, I discovered that the size of my new-found birth family was humongous. Beulah was one of 14 children, and some her siblings had equally large families.

The obituary for her father, Jim Frank Wooten, said he had 56 grandchildren! I had a lot of research to do if I were to find every 2nd cousin.

I still had those other close DNA matches to figure out. The closest match at FTDNA turned out to also be a Wooten whose grandmother was a sister to Jim Frank Wooten, my birth great grandfather.

The closest match who responded at 23andMe was related to the Langston line, through marriage to my birth great grandmother, a Williams.

I was thus able to triangulate, if you will, my closest matches at all three companies.

On occasion, I contacted other Ancestry members whose family trees showed promise but weren’t clear. One contact was to the wife of a nephew of an apparent 2nd cousin, one of 13 children of Matthew James Wooten, one of Beulah’s brothers. There was a different first name on her family tree than what I had found in my research. She responded and confirmed they were the same person, her husband’s aunt, and said she would contact her and provide my contact information.

One thing led to another, and I wound up talking with one of Matthew James Wooten’s sons. He, a sister and another cousin were vacationing in Florida, and we agreed to meet.

Of course I came prepared to argue my case before the Supreme Court with all the evidence I had accumulated up to that point. But they took one look at me and decided I was a Wooten after all. I gave them copies of my DNA reports in case others in the family had their doubts.

After all, how does someone pop up after 62 years claiming to be a son of someone who had three husbands and children by two of them?

They confirmed much of what I had found, such as knowing Elizabeth had spent time in Miami. We spent the entire day together talking about the family.

It was, as you can imagine, one of the most memorable, joyful days in my life; meeting family for the first time, one I never knew existed. They were warm and accepting, and I came away grateful I had started this search.

Decoration – A Southern Family Tradition

They told me about Decoration at the family cemetery, held each May in Trenton, Georgia. I knew I’d be attending no matter what.

Mark4

Decoration is an apparently Southern tradition I had not known about, one I find very compelling. It moreover serves as a family reunion where everyone gets together for a big feast after cleaning and decorating family headstones. I was able to attend and spent the previous week exploring the area near Chattanooga with its Civil War battlefields.

Of course I wondered how I would be accepted. I needn’t have. In fact, I was kind of an honored guest and welcomed with open hearts and lots of food.

Lots of food, especially deviled eggs.

One cousin remarked that if I had shown up as some skinny little thing they would have had doubts, but seeing I was “full-bodied” I fit right in

Mark5

Jeanene attended with her mother (above), as did many of the children of Matthew James Wooten from Virginia, some of whom I had not yet met. The Wooten cousin that was my closest match at FTDNA also attended from Alabama.

There were cousins galore, some 70-80 people at the community center in Trenton, including two first cousins, the daughters of one of Elizabeth’s half-brothers. We exchanged information and agreed to stay in touch.

Mark6

I wish I could remember the names of all the cousins I met, but I thought it would be rude to carry around a notebook.

And the old family photos! There was one of my birth mother at an earlier Decoration and several older photos of my birth-grandmother before she passed in 1957. I took several photos of photos with my cellphone.

I now can place a face with a name and keep in contact with cousins I never knew I had.

The Circle

One disappointment though; no one had had any communication for several years with my two possibly living half-sisters, or their families.

The circle was not yet complete, if it ever would be.

People say you can choose friends but not family. This is only partially true. Some of us have a choice when faced with the knowledge that a family exists out there that has no clue of our existence.

I wonder what it would be like to come to know the siblings I might still have.

The ambivalence is profound.

It’s like First Contact with an alien civilization, having found one a few light years from Earth; do we make contact not knowing what the response would be. But we as human beings have this insatiable need to explore the unknown and ask questions and take actions that may be very risky. It’s in our genes, if you will.

I have to ponder this for a while….

Hope Through Genetics

I’d like to thank Roberta for affording me this opportunity of sharing my quest to answer “the question.” I’ve followed her blog for some three years now and have found her own stories of family search truly inspiring, and appreciate her words of encouragement in my search.

We all seek to find out more of where we come from.

Adoptees and others who have lost contact with family now have hope through genetics to find the answer. We all look forward to the day when we can pinpoint where on Earth our ancestors came from. It might even be the Orkneys.

Mark

DNA Testing Strategy for Adoptees and People with Uncertain Parentage

Adoptees aren’t the only people who don’t know who their parents are.  There are many people who don’t know the identity of one of their two parents…and it’s not always the father.  Just this week, I had someone who needed to determine which of two sisters was her mother.  Still, the “who’s your Daddy” crowd, aside from adoptees, is by far the largest.

The DNA testing strategy for both of these groups of people is the same, with slight modifications for male or female. Let’s take a look.

Males have three kinds of DNA that can be tested and then compared to other participants’ results.  The tests for these three kinds of DNA provide different kinds of information which is useful in different ways.  For example, Y DNA testing may give you a surname, if you’re a male, but the other two types of tests can’t do that, at least not directly.

Females only have two of those kinds of DNA that can be tested.  Females don’t have a Y chromosome, which is what makes males male genetically.

adopted pedigree

If you look at this pedigree chart, you can see that the Y chromosome, in blue, is passed from the father to the son, but not to daughters.  It’s passed intact, meaning there is no admixture from the mother, who doesn’t have a Y chromosome, because she is female.  The Y chromosome is what makes males male.

The second type of DNA testing is mitochondrial, represented by the red circles.  It is passed from the mother to all of her children, of both genders, intact – meaning her mitochondrial DNA is not admixed with the mtDNA of the father.  Woman pass their mtDNA on to their children, men don’t.

Therefore when you test either the Y or the mtDNA, you get a direct line view right down that branch of the family tree – and only that direct line on that branch of the tree.  Since there is no admixture from spouses in any generation, you will match someone exactly or closely (allowing for an occasional mutation or two) from generations ago.  Now, that’s the good and the bad news – and where genealogical sleuthing comes into play.

On the chart above, the third kind of DNA testing, autosomal DNA, tests your DNA from all of your ancestors, meaning all of those boxes with no color, not just the blue and red ones, but it does include the blue and red ancestors too.  However, autosomal DNA (unlike Y and mtDNA) is diluted by half in each generation, because you get half of your autosomal DNA from each parent, so only half of the parents DNA gets passed on to each child.

Let’s look at how these three kinds of DNA can help you identify your family members.

Y DNA

Since the Y DNA typically follows the paternal surname, it can be extremely helpful for males who are searching for their genetic surname.  For example, if your biological father’s surname is Estes, assuming he is not himself adopted or the product of a nonpaternal event (NPE) which I like to refer to as undocumented adoptions, his DNA will match that of the Estes ancestral line.  So, if you’re a male, an extremely important test will be the Y DNA test from Family Tree DNA, the only testing company to offer this test.

Let’s say that you have no idea who your bio-father is, but when your results come back you see a preponderance of Estes men whom you match, as well as your highest and closest matches being Estes.

By highest, I mean on the highest panel you tested – in this case 111 markers.  And by closest, I mean with the smallest genetic distance, or number of mutations difference.  On the chart below, this person matches only Estes males at 111 markers, and one with only 1 mutation difference (Genetic Distance.)  Please noted that I’ve redacted first names.

Hint for Mr. Hilbert, below – there is a really good chance that you’re genetically Estes on the direct paternal side – that blue line.

Estes match ex

The next step will be to see which Estes line you match the most closely and begin to work from there genealogically.  In this case, that would be the first match with only one difference.  Does your match have a tree online?  In this case, they do – as noted by the pedigree chart icon.  Contact this person.  Where did their ancestors live?  Where did their descendants move to?  Where were you born?  How do the dots connect?

The good news is, looking at their DNA results, you can see that your closest match has also tested autosomally, indicated by the FF icon, so you can check to see if you also match them on the Family Finder test utilizing the Advanced Matching Tool.  That will help determine how close or distantly related you are to the tester themselves.  This gives you an idea how far back in their tree you would have to look for a common ancestor.

Another benefit is that your haplogroup identifies your deep ancestral clan, for lack of a better word.  In other words, you’ll know if your paternal ancestor was European, Asian, Native American or African – and that can be a hugely important piece of information.  Contrary to what seems intuitive, the ethnicity of your paternal (or any) ancestor is not always what seems evident by looking in the mirror today.

Y DNA – What to order:  From Family Tree DNA, the 111 marker Y DNA test.  This is for males only.  Family Tree DNA is the only testing company to provide this testing.  Can you order fewer markers, like 37 or 67?  Yes, but it won’t provide you with as much information or resolution as ordering 111 markers.  You can upgrade later, but you’ll curse yourself for that second wait.

FTDNA Y

Mitochondrial DNA

Males and females both can test for mitochondrial DNA.  Matches point to a common ancestor directly up the matrilineal side of your family – your mother, her mother, her mother – those red circles on the chart.  These matches are more difficult to work with genealogically, because the surnames change in every generation.  Occasionally, you’ll see a common “most distant ancestor” between mitochondrial DNA matches.

Your mitochondrial DNA is compared at three levels, but the most accurate and detailed is the full sequence level which tests all 16,569 locations on your mitochondria.  The series of mutations that you have forms a genetic signature, which is then compared to others.  The people you match the most closely at the full sequence level are the people with whom you are most likely to be genealogically related to a relevant timeframe.

You also receive your haplogroup designation with mitochondrial DNA testing which will place you within an ethnic group, and may also provide more assistance in terms of where your ancestors may have come from.  For example, if your haplogroup is European and you match only people from Norway….that’s a really big hint.

Using the Advanced Matching Tool, you can also compare your results to mitochondrial matches who have taken the autosomal Family Finder test to see if you happen to match on both tests.  Again, that’s not a guarantee you’re a close relative on the mitochondrial side, but it’s a darned good hint and a place to begin your research.

Mitochondrial DNA – What to Order:  From Family Tree DNA, the mitochondrial full sequence test.  This is for males and females both.  Family Tree DNA is the only company that provides this testing.

FTDNA mtDNA

Autosomal DNA

Y and mitochondrial DNA tests one line, and only one line – and shoots like a laser beam right down that line, telling you about the recent and deep history of that particular lineage.  In other words, those tests are deep and not wide.  They can tell you nothing about any of your other ancestors – the ones with no color on the pedigree chart diagram – because you don’t inherit either Y or mtDNA from those ancestors.

Autosomal DNA, on the other hand tends to be wide but not deep.  By this I mean that autosomal DNA shows you matches to ancestors on all of your lines – but only detects relationships back a few generations.  Since each child in each generation received half of their DNA from each parent – in essence, the DNA of each ancestor is cut in half (roughly) in each generation.  Therefore, you carry 50% of the DNA of your parents, approximately 25% of each grandparent, 12.5% of the DNA of each great-grandparent, and so forth.  By the time you’re back to the 4th great-grandparents, you carry only about 1% of the DNA or each of your 64 direct ancestors in that generation.

What this means is that the DNA testing can locate common segments between you and your genetic cousins that are the same, and if you share the same ancestors,  you can prove that this DNA in fact comes from a specific ancestor.  The more closely you are related, the more DNA you will share.

Another benefit that autosomal testing provides is an ethnicity prediction.  Are these predictions 100% accurate?  Absolutely not!  Are they generally good in terms of identifying the four major ethnic groups; African, European, Asian and Native American?  Yes, so long at the DNA amounts you carry of those groups aren’t tiny.  So you’ll learn your major ethnicity groups.  You never know, there may be a surprise waiting for you.

FTDNA myOrigins

The three vendors who provide autosomal DNA testing and matching all provide ethnicity estimates as well, and they aren’t going to agree 100%.  That’s the good news and often makes things even more interesting.  The screen shot below is the same person at Ancestry as the person above at Family Tree DNA.

Ancestry ethnicity

If you’re very lucky, you’ll test and find an immediate close match – maybe even a parent, sibling or half-sibling.  It does happen, but don’t count on it.  I don’t want you to be disappointed when it doesn’t happen.  Just remember, after you test, your DNA is fishing for you 24X7, every single hour of every single day.

If you’re lucky, you may find a close relative, like an uncle or first cousin.  You share a common grandparent with a first cousin, and that’s pretty easy to narrow down.  Here’s an example of matching from Family Tree DNA.

FTDNA close match

If you’re less lucky, you’ll match distantly with many people, but by using their trees, you’ll be able to find common ancestors and then work your way forward, based on how closely you match these individuals, to the current.

Is that a sometimes long process?  Yes.  Can it be done?  Absolutely.

If you are one of the “lottery winner” lucky ones, you’ll have a close match and you won’t need to do the in-depth genealogy sleuthing.  If you are aren’t quite as lucky, there are people and resources to help you, along with educational resources.  www.dnaadoption.com provides tools and education to teach you how to utilize autosomal DNA tools and results.

Of course, you won’t know how lucky or unlucky you are unless you test.  Your answer, or pieces of your answer, may be waiting for you.

Unlike Y and mtDNA testing, Family Tree DNA is not the only company to provide autosomal of testing, although they do provide autosomal DNA testing through their Family Finder test.

There are two additional companies that provide this type of testing as well, 23andMe and Ancestry.com.  You should absolutely test with all three companies, or make sure your results are in all three data bases.  That way you are fishing in all of the available ponds directly.

If you have to choose between testing companies and only utilize one, it would be a very difficult choice.  All three have pros and cons.  I wrote about that here.  The only thing I would add to what I had to say in the comparison article is that Family Tree DNA is the only one of the three that is not trying to obtain your consent to sell your DNA out the back door to other entities.  They don’t sell your DNA, period.  You don’t have to grant that consent to either Ancestry or 23andMe, but be careful not to click on anything you don’t fully understand.

Family Tree DNA accepts transfers of autosomal data into their data base from Ancestry.  They also accept transfers from 23andMe if you tested before December of 2013 when 23andMe reduced the number of locations they test on their V4 chip

Autosomal DNA:  What to Order

Ancestry.com’s DNA product at http://www.ancestry.com – they only have one and it’s an autosomal DNA test

23andMe’s DNA product at http://www.23andMe.com – they only have one and it’s an autosomal DNA test

Family Tree DNA – either transfer your data from Ancestry or 23andMe (if you tested before December 2013), or order the Family Finder test. My personal preference is to simply test at Family Tree DNA to eliminate any possibility of a file transfer issue.

FTDNA FF

Third Party Autosomal Tools

The last part of your testing strategy will be to utilize various third party tools to help you find matches, evaluate and analyze results.

GedMatch

At GedMatch, the first thing you’ll need to do is to download your raw autosomal data file from either Ancestry or Family Tree DNA and upload the file to www.gedmatch.com.  You can also download your results from 23andMe, but I prefer to utilize the files from either of the other two vendors, given a choice, because they cover about 200,000 additional DNA locations that 23andMe does not.

Ancestry.com provides you with no tools to do comparisons between your DNA and your matches.  In other words, no chromosome browser or even information like how much DNA you share.  I wrote about that extensively in this article, and I don’t want to belabor the point here, other than to say that GedMatch levels the playing field and allows you to eliminate any of the artificial barriers put in place by the vendors.  Jim Bartlett just wrote a great article about the various reasons why you’d want to upload your data to Gedmatch.

GedMatch provides you with many tools to show to whom you are related, and how.  Used in conjunction with pedigree charts, it is an invaluable tool.  Now, if we could just convince everyone to upload their files.  Obviously, not everyone does, so you’ll still need to work with your matches individually at each of the vendors and at GedMatch.

GedMatch is funded by donations or an inexpensive monthly subscription for the more advanced tools.

DNAGEDCOM.com

Another donation based site is http://www.dnagedcom.com which offers you a wide range of analytical tools to assist with making sense of your matches and their trees.  DNAGEDCOM works closely with the adoption community and focuses on the types of solutions they need to solve their unique types of genealogy puzzles.  While everyone else is starting in the present and working their way back, adoptees are starting with the older generations and piecing them together to come forward to present.  Their tools aren’t just for adoptees though.  Tools such as the Autosomal DNA Segment Analyzer are great for anyone.  Visit the site and take a look.

Third Party Y and Mitochondrial Tools – YSearch and MitoSearch

Both www.ysearch.org and www.mitosearch.org are free data bases maintained separately from Family Tree DNA, but as a courtesy by Family Tree DNA.  Ysearch shows only a maximum of 100 markers for Y DNA and Mitosearch doesn’t show the coding region of the mitochondrial DNA, but they do allow users to provide their actual marker values for direct comparison, in addition to other tools.

Furthermore, some people who tested at other firms, when other companies were doing Y and mtDNA testing, have entered their results here, so you may match with people who aren’t matches at Family Tree DNA.  Those other data bases no longer exist, so Ysearch or Mitosearch is the only place you have a prayer of matching anyone who tested elsewhere.

You can also adjust the match threshold so that you can see more distant matches than at Family Tree DNA.  You can download your results to Ysearch and Mitosearch from the bottom of your Family Tree DNA matches page.

Mitosearch upload

Answer the questions at Mito or Ysearch, and then click “Save Information.”  When you receive the “500” message that an error has occurred at the end of the process, simply close the window.  Your data has been added to the data base and you can obtain your ID number by simply going back to your match page at Family Tree DNA and clicking on the “Upload to Ysearch” or Mitosearch link again on the bottom of your matches page.  At that point, your Y or mitosearch ID will be displayed.  Just click on “Search for Genetic Matches” to continue matching.

Get Going!

Now that you have a plan, place your orders and in another 6 to 8 weeks, you’ll either solve the quandry or at least begin to answer your questions.  Twenty years ago you couldn’t have begun to unravel your parentage using DNA.  Now, it’s commonplace.  Your adventure starts today.

Oh, and congratulations, you’ve just become a DNA detective!

I wish you success on your journey – answers, cousins, siblings and most importantly, your genetic family.  Hopefully, one day it will be you writing to me telling me how wonderful it was to meet your genetic family for the first time, and what an amazing experience it was to look across the dinner table and see someone who looks like you.

Baby Boy Hacht – Born July 1944 – Dead, or Kidnapped and Alive Today??

A baby boy who was never named was born in July 1944, in Detroit, Michigan.  The family believes that he was kidnapped and another dead baby substituted for Baby Boy Hacht.  While at first this sounds improbable, if not incredulous, it isn’t.

That child, if still living, would be 70 today.  So, if you or a male family member was born in the summer of 1944, in or near Detroit, please consider this possibility as you read this article.  It’s also possible that if the child was part of a black market baby ring, the birth location could have been falsified, so any birth in late July 1944 should be considered.

What Happened?

John James Hacht & Jean Marie Mlasko were married on November 18, 1942 in  Michigan.
hacht wedding

In 1943, Jean became pregnant, and in the heat of the summer in 1944, on July 29th, their first child, a boy was born at Grace Hospital, a Catholic hospital, in Detroit.

This date is very important, as is the fact that the hospital was Catholic as this story unfolds.

I met Patti Hacht, the sister of Baby Boy Hacht, in 2009.  We worked on this mystery for some time, but have hit a dead end.  Patti’s living brother tested at Family Tree DNA for the Y DNA and Patti has tested at Family Tree DNA, 23andMe and at Ancestry for autosomal DNA.

I’ve asked Patti to tell this story in her own words.

On 29 July 1944 a first child was born to my parents – a son who never received a name other than Baby Boy Hacht (BBH.) BBH was born at Grace Hospital in Detroit, Michigan. My mom fed him for several days and then one day “medical personnel” came in and told her that her baby had died.

BBH had not been ill, and my dad’s sister worked at Grace Hospital. These three family members never believed BBH died. They always believed he was “switched” with another baby, one that really had died.  My mother did not see the baby after death, but my father did, and he never believed the dead child was his child.

When I first heard of BBH, I was in my mid-late 40’s. I was driving in the car with my mother one day as we were driving by White Chapel Cemetery, about a year before she died, and she casually said, “That’s where our first baby is buried,” then added, “but we never believed our baby died.”  I almost drove off the freeway!

First baby?

Died????

Didn’t die??

Wha…..???

It took me 3 years to find BBH at White Chapel.  As it turns out, he was not buried there.  He was cremated there, but his cremains were sent back to the funeral director.

Having been a family researcher for over 30 years, I went to the Detroit Vital Records Department to get a Death Certificate for BBH. As I walked away from the counter, reading this new document, I saw that BBH was listed as “stillborn.”

Stillborn???

That was impossible.

You can’t feed a stillborn baby for “several days.”

BBH Death

So I went back to the counter, hoping to find out what was going on with this “wrong” Death Certificate. The clerk suggested we look for a Birth Record.

Ten minutes later, we had that record, and it too stated that BBH was “stillborn.”  I later discovered that a stillborn baby never received a birth certificate at that time, only a death certificate.  In 2003, Michigan began issuing Certificates of Stillbirth in addition to death certificates.

BBH birth

On closer inspection, it was clear that the Certificate of Death had been heavily altered. Someone had taken what appeared to be a thin Scripto pen (which had not even been invented yet in 1944) and “wrote over” what had originally been written on the document. The written over date was “29”, the year was “44” and the time was “9:57 a.m.”

Additionally, except for the signatures, all of the other information for BBH was typed, except for the birth date and death information…almost like the death certificate was being pre-prepared.

BBH modification

I noticed another odd detail – BBH had been cremated. This was unheard of in this timeframe and was expressly prohibited by the Catholic church.  Grace was a Catholic hospital.  My parents were actively Catholic.  All of their children attended Catholic school.  White Chapel Cemetery, where the cremation occurred told me that they would have only cremated “maybe one person” a year in 1944, and never a newborn baby.

However, his certificate clearly states that BBH was cremated.

For several years I tried to find the funeral home, J. P. Miller on Van Dyke in Detroit. Apparently my parents never picked up BBH’s cremains, apparently because they believed he had been buried, and I wondered if I might find viable DNA in them.

After about four years, I talked with someone at the funeral home. It had been sold a couple times, and the man I spoke with was retiring the very day I had called. He said that any cremains that might have remained in the building would have been destroyed as the building had been abandoned for several years and the roof had collapsed, so the inside of the building was exposed to the elements for many years.

I wondered why my Catholic family would have cremated their child and why they never picked up the cremains or had them buried.  It makes sense only in the context that my parents never believed the dead child was their son and they sent the child’s remains who were substituted for their own child’s to be handled in the least expensive way possible.  They likely had no idea that the child’s cremains weren’t buried and were returned to the funeral home.  They never visited the grave because they never believed their child died.  Unfortunately, by the time all of the details unfolded, my parents had passed away and couldn’t be asked.

This was also a very difficult time for the family for other reasons as well.  My father’s mother was terminal with cancer and would die a couple of months later.  This young couple had their hands full.

For several years the family pondered over those “write overs” in BBH’s Certificate of Death. In April of 2006 we hired Speckin Forensic Laboratory in Okemos, Michigan to conduct a forensic exam on BBH’s original Death Certificate – we wanted to know what had been “written over.” Getting to the exam had been a lengthy process. I was appointed BBH’s Personal Representative in Probate Court, and we had to obtain a court order for the State of Michigan to allow the forensic exam.

The forensic exam showed three chemical erasures – someone used some sort of chemical to first try to “erase” what had originally been written. Then they just wrote right over those chemical erasures. The original writings were: Day, 31 July. (This had been overwritten to read “29” July); Time, 10:00 a.m. (This had been overwritten to read “9:57 a.m.) So the date was changed from 31 July to 29 July and the time was changed from 10 a.m. to 9:57 a.m.  The exam also clearly showed that the “overwritten” information was written with a different ink that the original writing.

Death Day Death Time
Original Entry July 31 10 AM
Overwritten Entry July 29 9:57 AM

It was the opinion of the examiner (who was a retired Michigan State Police Officer) that the Certificate of Death was probably altered to “match” BBH’s Certificate of Birth. There probably was a baby that died and for whatever reason, and this baby probably died on 31 July. Then BBH was “substituted” for this deceased baby, and records were created that would make BBH’s Certificate of Birth and Certificate of Death “match.”  If his birth and death date and time didn’t match, by three minutes, then he wasn’t “stillborn.”

speckin 1

speckin 2

The Detroit Legal News at that time published all the births in Wayne County. The males and females each had their own column, and the name and address of the mother was listed, along with the date of her child’s birth. I have compiled a list of about 200 male births in all of Wayne County from 27 July through 31 July. I believe one of these mothers took BBH home from the hospital and raised him as her own. She may have never known BBH was not her biological child.

I have been trying for years to narrow this list of 200+ names to ONLY babies born at Grace Hospital. All attempts to accomplish this have proved unsuccessful.  Hospital records reportedly “burned” several years ago.

St. Patrick’s Catholic Church on Parson’s Street in Detroit would have been the Church that handled emergency baptisms for babies born at Grace Hospital – babies that became ill and needed to be baptized immediately. The baby baptized would have been one of those babies on my list of 200+ names from the Detroit Legal News. St. Patrick’s records do not have a baptism for BBH or any of the other names on my list. I do not know if you had to be Catholic to deliver a baby at Grace Hospital. Perhaps the baby that really died was not born to Catholic parents, so there would not be a record of a Catholic baptism?  A stillborn baby is not baptized either.

We don’t know WHY Baby Boy Hacht was substituted for a deceased baby. Were the dead baby’s parents from an elite Detroit area family? A member of the Mob? Was it someone that hospital personnel was afraid to inform that their baby had died?  Were hospital personnel negligent with someone else’s baby and decided to switch the dead baby for BBH, thinking these were young parents and they could just have another baby the next year? Did BBH become part of a black market baby ring?  Why was the death certificate backdated to say that BBH was stillborn instead of having died 2 days later?

Or was there perhaps a widow whose husband had just been killed in WWII who  delivered a stillborn baby and doctors determined to “fix” the situation for a new widow? This last idea was nixed – as in 1944, the thinking was more “stiff upper lip” and people did not necessarily treat the bereaved gently.  The thinking of the day was to “get on with your life”, and giving a recent widow someone else’s baby didn’t mesh with that way of thinking.

Possibilities

If something wasn’t being covered up, then why were the dates and time changed, and why was a child who had lived for 2 days listed as stillborn?

Let’s take a look at scenarios of different possibilities.

  • One Time Baby Swap – The baby of another patient died or was stillborn on the 31st and BBH was swapped for that child. If this is the case, then the swap was unplanned and the mother was likely from the area. BBH’s paperwork was altered to reflect that he was the stillborn child, on the 29th, not on the 31st as originally recorded on his death certificate.
  • BBH Died of Natural Causes – If BBH simply died, the hospital would have completed a death certificate and not gone to the trouble to falsify his death certificate, claiming a still birth to match his birth certificate time and date.
  • BBH Died of an Accident by Hospital Staff – Let’s say someone on the hospital staff accidentally dropped the baby and the baby died. This might get sticky and making the death a stillbirth, which was much more common, would avoid any questions.
  • BBH Died of an Accident by His Parents – Let’s say one of his parents accidentally dropped the baby at the hospital and he died. In this case, the hospital would certainly not have been complicit in a coverup and would not have falsified the death certificate, nor claimed that the child was stillborn. There would have been a death certificate that reflected the actual death date and cause, and not a stillbirth.
  • BBH Was Part of a Larger Baby Market Ring – In this case, the couple who raised BBH as their own would not have necessarily been from the Detroit area. Young and naïve parents would have been the best targets as they would be less likely to ask questions and/or make waves. This would also have required the involvement of at least one doctor (to sign death certificates) and more likely several medical personnel including nurses. However, this would have been much more effective if the child was simply spirited away at birth and the parents told the child was dead, not after the parents having handled the child for “several days.” Given that BBH’s paternal aunt worked at that hospital, if there was something of this nature, you would think that over the years she would have at least heard rumblings, especially given that the family, including her, believed that BBH had been swapped for a dead child.

Either the One Time Baby Swap or the Accidental Death by Hospital Staff make the most sense.  If the BBH was swapped, as his parents and family believed, then he may be alive today.

It’s very possible that the parents who raised BBH had no idea what happened, and therefore, neither does BBH himself.

Babies Born in Detroit

I asked Patti to provide the various documents involved, as well as the names of the other families who were listed as having given birth in the Detroit area in the surrounding days.

It’s most likely that the baby that died passed away on July 31st and that BBH’s death certificate was amended on July 31st, as the original writing stated, to reflect that he was stillborn on July 29th instead.  Although, I certainly have to wonder if the doctor who signed as the attending physician didn’t think that the parents would have noticed at the discrepancy – especially since the child had been attended by his parents for part of the 29th, the 30th and the 31st until he “died.”  At that time, however, one simply did not question someone like a doctor.

Perhaps the amendment was actually done after the doctor signed the original death certificate, but that is unlikely, because a cause of death would have been completed by the doctor and there is no other cause of death listed other than stillborn, which was unquestionably not true.

In any event, this first list is the list of surnames of families whose children were born in Wayne County on July 31st.  The 31st is the most likely day for the baby who was stillborn to have been born since that is the original death certificate date on BBH’s death certificate.  There is no way to determine which of these babies were born at Grace Hospital.

Also, please keep in mind that this list is very likely incomplete – births of illegitimate children and children who died weren’t listed.  Others, such as famous or notorious people, may not have been listed either.  The hospital was very clearly in control of which births were submitted for publication, and which were not – and if there was something “funny” about the birth of BBH or the other child – or the parents were famous or infamous, that birth may not have been listed.  It’s also possible that the parents who wound up with BBH were not from Detroit.

  • Akin
  • Bailey
  • Bennett
  • Boytim
  • Brow
  • Bruce
  • Cappo
  • Craver
  • Davis
  • Dellamore
  • Dinneweth
  • Downes
  • DuBois
  • Elmasian
  • Faron
  • Fletcher
  • Flood
  • Gampel
  • Grandmaison
  • Harter
  • Hicks
  • Hill
  • Jones
  • Karas
  • Kekaha
  • Koblicz
  • Kraemer
  • Liss.
  • Mitchell
  • Nadolny
  • Pospeshil
  • Quiroz
  • Ready
  • Rotenberg
  • Rutzel
  • Shoemaker
  • Shoemaker
  • Smith
  • Stallings
  • Swartz
  • Thompson
  • William
  • Zimostrad

This second list includes the surnames of all of the babies born in Wayne County between July 27 and July 31, 1944 with the municipality as listed in the birth announcements in the newspaper.

7/30 Acker Detroit
7/30 Ackerman East Detroit
7/31 Akin Detroit
7/29 Anderson Detroit
7/29 Ash Detroit
7/31 Bailey Dearborn
7/27 Bartlett
7/28 Bawiee Detroit
7/27 Bazell Detroit
7/27 Beninati Detroit
7/31 Bennett Detroit
7/29 Bills Detroit
7/30 Blankenship Detroit
7/28 Bobo Detroit
7/27 Bombalski Detroit
7/30 Bond Detroit
7/28 Boorgois Gr. Pte Woods
7/28 Bourgeois Detroit
7/28 Bowman Detroit
7/29 Bowser Detroit
7/29 Boyce Detroit
7/29 Boyd Detroit
7/31 Boytim Centerline
7/29 Brantley Detroit
7/30 Brenner Detroit
7/27 Briggs Detroit
7/31 Brow Hazel Park
7/28 Brown Detroit
7/27 Brownlee Detroit
7/31 Bruce Detroit
7/30 Burchby Detroit
7/27 Burges Detroit
7/28 Burley Highland Park
7/30 Canfield Detroit
7/31 Cappo Dearborn
7/29 Carswell Detroit
7/27 Chobot Dearborn
7/28 Ciavone Detroit
7/27 Clifton Detroit
7/27 Coba Dearborn
7/29 Common Detroit
7/28 Cook Redford
7/27 Cooper Detroit
7/31 Craver Detroit
7/28 Crichton Detroit
7/29 Cromwell Grosse Pointe
7/27 Cummins Detroit
7/27 Davidson Detroit
7/28 Davio Detroit
7/31 Davis Detroit
7/31 Dellamore Detroit
7/28 Dennis Detroit
7/27 Deraedt Detroit
7/29 Dilda Detroit
7/31 Dinneweth Detroit
7/28 Donati Detroit
7/31 Downes Detroit
7/31 DuBois Detroit
7/27 Dunn Detroit
7/27 Earl Detroit
7/28 Ehrisman Detroit
7/28 Eldridge Ferndale
7/31 Elmasian Detroit
7/29 Engel Detroit
7/28 Ettinger Detroit
7/29 Fane Detroit
7/31 Faron Detroit
7/28 Fenstermacher Detroit
7/31 Fletcher Detroit
7/31 Flood Inkster
7/27 Fontana Detroit
7/29 Fung Yee Detroit
7/31 Gampel Detroit
7/29 Garrett Detroit
7/30 George Detroit
7/28 Glasnier Detroit
7/28 Gondos Detroit
7/31 Grandmaison Detroit
7/29 Greggie Birmingham
7/28 Griem Detroit
7/27 Gualdoni Detroit
7/30 Gunderson Detroit
7/29 Gurski Detroit
7/30 Hagerstrom Detroit
7/28 Harris Detroit
7/31 Harter Detroit
7/27 Haugh Detroit
7/27 Heiner Detroit
7/31 Hicks Detroit
7/28 Higgens Detroit
7/31 Hill North Carolina
7/30 Hillier Redford
7/27 Husak Detroit
7/28 Hussett Detroit
7/30 Ilby Plymouth
7/29 Jackson Detroit
7/30 Jackson Inkster
7/30 Jerimias Royal Oak
7/31 Jones Detroit
7/27 Jorden Detroit
7/30 Jozsa Detroit
7/28 July Van Dyke (??)
7/27 Kaczmarczyk Detroit
7/29 Kampa Detroit
7/31 Karas Detroit
7/30 Kaump Detroit
7/31 Kekaha Hazel Park
7/27 Kibler Detroit
7/27 Kilgore Highland Park
7/27 Kipp Royal Oak
7/31 Koblicz Detroit
7/27 Koerber Detroit
7/28 Kolongowski Detroit
7/31 Kraemer Detroit
7/27 Kuczenski Detroit
7/30 Kujawski Detroit
7/28 LaRose Detroit
7/28 Larsen Detroit
7/28 Leland Detroit
7/29 Lennert Detroit
7/29 Lightle Wyandotte
7/30 Lisiecki Hamtramak
7/31 Liss. Dearborn
7/30 Lovince Hamtramak
7/29 Lubs Allen Park
7/30 Lucey Grosse Pt. Park
7/27 Lupo Detroit
7/28 Malczyk Detroit
7/28 Maloney Detroit
7/29 Martin Detroit
7/30 Martin Detroit
7/30 Matley Detroit
7/30 Mattei Detroit
7/29 Mc Flgunn Detroit
7/28 Mc Millan Detroit
7/30 Meisner Detroit
7/27 Mitchell Detroit
7/28 Mitchell Grosse Pointe
7/29 Mitchell Ferndale
7/31 Mitchell Detroit
7/29 Moore Farmington
7/30 Moore Farmington
7/30 Morehead Inkster
7/27 Moses Detroit
7/31 Nadolny Allen Park
7/27 Neilson Detroit
7/30 Neu. Detroit
7/29 Noder Detroit
7/28 Nowakowski Detroit
7/27 Or Detroit
7/28 Pacult Detroit
7/29 Palmer Berkley
7/29 Parker Inkster
7/30 Parr Detroit
7/29 Peguese Detroit
7/29 Perri Dearborn
7/31 Pospeshil Detroit
7/30 Powell Detroit
7/27 Prange Detroit
7/31 Quiroz Detroit
7/27 Rabidue Detroit
7/30 Randolph Detroit
7/27 Ranin Detroit
7/31 Ready Detroit
7/29 Reiss Detroit
7/28 Rey Mt. Clemens
7/30 Rhodes Detroit
7/28 Richardson Detroit
7/27 Roberts Detroit
7/31 Rotenberg Detroit
7/28 Roush Detroit
7/31 Rutzel Detroit
7/30 Ryback Detroit
7/29 Rychlicki Detroit
7/29 Scafero Detroit
7/29 Schart Detroit
7/27 Schneider Detroit
7/30 Scott Detroit
7/28 Serling Detroit
7/29 Sevener Grosse Pt. Park
7/29 Shackney Detroit
7/27 Shipley Ferndale
7/31 Shoemaker Farmington
7/31 Shoemaker Detroit
7/28 Sievert Dearborn
7/29 Simm Detroit
7/27 Slavko Detroit
7/28 Smith Detroit
7/29 Smith Detroit
7/31 Smith Detroit
7/30 Springer Detroit
7/31 Stallings Detroit
7/27 Stanton Detroit
7/29 Stefanic Detroit
7/28 Steiner Detroit
7/29 Stepulla Hamtramak
7/27 Stoven Detroit
7/31 Swartz Detroit
7/28 Tekel Melvindale
7/27 Terhaar Detroit
7/31 Thompson Detroit
7/28 Towe Detroit
7/29 Tromburrini Detroit
7/28 Trouttchaud Dearborn
7/27 Turner Detroit
7/27 Vitagliano Detroit
7/27 Voss Detroit
7/27 Watkins Detroit
7/29 Watson Hazel Park
7/30 Wenban Detroit
7/29 Westland Detroit
7/27 Wheeler Detroit
7/29 Whitman Detroit
7/31 William Detroit
7/28 Williams Detroit
7/30 Williams Detroit
7/29 Winfrey Detroit
7/29 Winters Detroit
7/28 Wolfbauer East Detroit
7/29 Wright Pleasant Ridge
7/30 Wyka Detroit
7/27 Yeszin Detroit
7/28 Yokubison Detroit
7/27 Zielinski Detroit
7/31 Zimostrad Wayne
7/30 Zink Birmingham
7/27 Zoulets Royal Oak

For additional information, contact Patti Hacht at duncaha@gmail.com.  Patti does have additional information about each family from the birth announcements.

What Might Baby Boy Hacht Have Looked Like?

This first photo is of two of BBH’s siblings, as children.

Patti & Jimmy Hacht

This second photo is of the 4 Hacht siblings as adults.

Colleen, Mark (back) Jimmy & Patti Hacht

Contact

If you think you might be Baby Boy Hacht, or might know of someone who would be a candidate – please contact Patti Hacht at duncaha@gmail.com.  Patti does have additional information about these families, such as the mother’s first name and the addresses.

If you would like to DNA test first to see if you match Patti’s brother’s Y DNA or Patti’s family by autosomal DNA, please test at Family Tree DNA.

The Y chromosome is passed from father to son intact and is what makes males male.  BBH carries his father’s Y chromosome and BBH’s sons would carry his.

Autosomal DNA is contributed to a child from both parents.  The child receives half of the DNA of both of his parents.  You can read more about how DNA is used for genetic genealogy here.

The Y DNA of Baby Boy Hacht or a his male child or male grandchild through a son will match that of Patti’s brother.  The autosomal DNA of Baby Boy Hacht or his children or grandchildren of any gender will match with Patti and her family.

If you would like to DNA test, we recommend the 37 marker Y DNA test at Family Tree DNA for males and the Family Finder autosomal test for either gender

Here’s the link if you’re interested.