I have never really studied genetics. I don’t have the right terminology for this. Apologies in advance.
First, I do know that all humans have the vast majority of their DNA in common. I assume there’s some term that refers to the rest – the part of DNA that varies from person to person. For simplicity’s sake, let’s just ignore the in-common part, and refer to the “varies by person“ part as just DNA.
As I understand it, a person gets half their DNA from each parent. If you did a 23-and-Me analysis on a parent and child, there would be a 50% match. (Of course, this assumes that the parents are not related to each other. If the parents are, say, first cousins or a Chinatown “She’s my mother! She’s my sister!” situation, there would likely be a greater than 50% match, no?)
(OK, thinking about this, I suddenly realized maybe that 50% business is always wrong. Parents share traits with each other. If mom and dad both have blue eyes, their offspring will have blue eyes, and rather than half of the child’s eye-color gene matching each parent, all of it will match each parent. Anyway, let’s ignore that and just go with 50%.)
So how much DNA do siblings have in common? My guess is that it should average 50%, but would probably be less or more than that.
Suppose Mary and John have a child they name Lee. We could divide Mary’s DNA into 2 groups: went to Lee (we’ll call that A), and didn’t go to Lee (B). Similarly John has DNA that went to Lee (C) and didn’t go to Lee (D). If Mary and John have another child (Chris), we’d assume that Chris’s DNA from Mary would be half A and half B, and from John would be half C and half D, so that Lee and Chris would share 50% of their DNA.
But that’s only an assumption. Isn’t it at least theoretically possible for Chris’s DNA to be all A and C (and therefore be basically a clone of Lee) or all B and D (and therefore genetically unrelated)? I realize the chance is miniscule, but isn’t the chance that Lee and Chris share exactly 50% of their DNA also miniscule?
I got to thinking about this due to a letter in Ask Amy this morning. It was about family turmoil being caused by genetic testing indicating that first cousins were in fact half-siblings. I’m thinking that in theory half-siblings should share 25% of their DNA, and first cousins should share 12.5%, but I’m also thinking it’s much more variable so that first cousins would be misidentified as half-siblings more often than people think. So how often would these misidentifications be likely to occur?
Also, do the DNA testing facilities have any prior knowledge about the relationship between the people whose DNA they are analyzing? Suppose Mary has a sister named Alice and John has a brother named Tom. If Alice and Tom have children, won’t those children show as more closely related to Lee and Chris than just first cousins?
TL:DR How much DNA is (Theoretically) shared by various family members?