Let's say we have a male with infertility issues. Him and his wife get a Chromosomal Analysis that comes back with his wife being fine, but him having:
"balanced reciprocal translocation between chromosomes one and ten"
46,XY,t(1;10)(q21;q25.2)
And the embryos from their first IVF round have the following abnormalities:
45,XY,dup(1)(q23q44),del(10)(q26),-22
46,XY,del(1)(q23),dup(10)(q26q26)
Why would the embryos have duplications and deletions on the same chromosome but at different locations than the abnormalities in the potential father?
