Got the results sheet, here goes:
Embryo 1 only had singles for chromosome 3, 9, 15, 16, 18, 20 & 22! It had an extra on 11 & 19! The other chromosomes were normal pairs.
Embryo 2 had an extra chromosome 4 & 16. Others were normal pairs.
Embryo 3 had an extra chromosome 8, all the rest normal pairs.
Embroyo 4 had an extra chromosome 1, 6, 10, 19 & XY/23. Only had a single for 2, 7, 16, 17 & 18. The rest were normal pairs.
Embryo 5 just had an extra chromosome 13, the rest normal pairs.
Embryo 6 only had a single for 10, 12, 15, 16, 21 & 22, the rest normal pairs.
Embryo 7 only had a single for chromosome 3 and had an extra for 9 and 22, the rest normal pairs.
Embryo 8 had an extra for chromosome 3 and only a single for 9 & 22, the rest normal pairs.
Ive been looking up what it all means. An extra chromosome for number 21 is Down Syndrome but a missing one causes birth defects or learning difficulties. One of them was for blood cancer and others have a huge list of diseases! It was really scary. Chromosome 8 duplication is associated with a lot of different syndromes. Chromosome 3 deletion is associated with autism. Im not sure what having 3 instead of a pair of sex chromosomes means either. I suppose it just means they cant join up properly and make a baby.
Very interesting but awful too.