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Originally Posted by
Maciamo
It's sad to see that after all this time on the forum you still don't understand what is mitochondrial DNA. You only inherited from a single mtDNA haplogroup. All the others in your ancestry are irrelevant.
Additionally, having an autosomal match (a few segments on one or several chromosomes) with an ancient individual doesn't mean that you inherited their mtDNA. Mitochondrial DNA is not nuclear DNA. It is not part of the 46 chromosomes. It is completely independent.
OK I understand. But IMO this tool gives a a picture of the whole ancestry. So the mtDNA of both of the grandmothers and their (grand-)mothers etc etc.
So mother split into the two grandmothers (one has the same MtDNA the other could be different) and so fort.
I hope I have made myself clear. And correct me if I am wrong.
Regarding my mother's result it has potential made a puzzle clear Maciamo!
In most PCA's (G25, most extreme in K36 results) she has got something Baltic. Based on this illustration this makes it clear, she has for modern standards a quite high component mtDNA I. Wiki:
The frequency of haplogroup I may have undergone a reduction in Europe following the Middle Ages. An overall frequency of 13% was found in ancient Danish samples from the Iron Age to the Medieval Age (including Vikings) from Denmark and Scandinavia compared to only 2.5% in modern samples.
And where is this actually high.....indeed the Baltics.