Hi everyone,
I took a Y-37 test a while ago (2011) and had no matches at 37 markers, none at 25 and even none at 12! More than 6 years later.. still the same!
I know that it can happen with some rarer haplogroups, but I'm R1b! More than that, R-M269 (as far as the Y-37 test results go, I know this can be narrowed down).
How likely is such a thing to happen, to have absolutely zero 12 markers match with the most common haplogroup in European populations? Is there anything interesting or significant that can be derived from it, other than the fact that no one else even remotely patrilinearly related (or not even) has taken the test? Would it be useful to post the specific number of repeats/unusual mutations that have taken place (there are some unusual ones, of course, hence the utter lack of matches), can they actually tell something, be revealing somehow?
Thanks a lot in advance for your answers!
I took a Y-37 test a while ago (2011) and had no matches at 37 markers, none at 25 and even none at 12! More than 6 years later.. still the same!
I know that it can happen with some rarer haplogroups, but I'm R1b! More than that, R-M269 (as far as the Y-37 test results go, I know this can be narrowed down).
How likely is such a thing to happen, to have absolutely zero 12 markers match with the most common haplogroup in European populations? Is there anything interesting or significant that can be derived from it, other than the fact that no one else even remotely patrilinearly related (or not even) has taken the test? Would it be useful to post the specific number of repeats/unusual mutations that have taken place (there are some unusual ones, of course, hence the utter lack of matches), can they actually tell something, be revealing somehow?
Thanks a lot in advance for your answers!
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