Notable Features |
Near-diploid with 12 structural abnormalities, some complex, involving chromosomes 1, 3, 4, 5, 6, 7, 8, 13, 14, 15, 18. Losses involve chromosomes 3p, 4, 5, 7, 20; partial gain of 15.
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46(45-49) XY, 1x1, der(1)t(1;4), 2x2, 3x1, der(3)t(5;3;7), der(3)t(3;5)(p12;p12), der(4)t(4;1;4;7), der(4)del(4)t(4;7), der(5)t(4;5), i(5p), der(5?)t(5;18), 6x2, der(6)t(6;8), 7x1, 8x2, 9x2, 10x2, 11x2, 12x2, 13x2, der(13)t(8;13), 14x2, 15x2, dup(15), 16x2, 17x2, 18x1, der(18)t(14;18;8), 19x2, 20x1, 21x2, 22x2
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