Pauline
LostCousins Megastar
When I first got my DNA results I tended to assume that if an unidentified match showed up as a shared match with a documented cousin, the unidentified match probably belonged in the same part of my tree.
Now, in the light of experience, I'm wondering just how safe this assumption might be, particularly when only one shared match shows up. More and more I'm finding occasions when a shared match is actually down to 'relatives in common', rather than all 3 of us having shared ancestry.
Sometimes this is easy to spot because an unidentified match has shared matches with known cousins in two (or more) unrelated parts of my tree. However, if there is just the one shared match it may not be apparent, and has the potential to mislead.
It's at times like this when I feel a chromosome browser would be a useful addition at Ancestry.
Have other people come across this problem much? Is it something that becomes more apparent as we gain more 'close cousin' matches?
Now, in the light of experience, I'm wondering just how safe this assumption might be, particularly when only one shared match shows up. More and more I'm finding occasions when a shared match is actually down to 'relatives in common', rather than all 3 of us having shared ancestry.
Sometimes this is easy to spot because an unidentified match has shared matches with known cousins in two (or more) unrelated parts of my tree. However, if there is just the one shared match it may not be apparent, and has the potential to mislead.
It's at times like this when I feel a chromosome browser would be a useful addition at Ancestry.
Have other people come across this problem much? Is it something that becomes more apparent as we gain more 'close cousin' matches?