Notable Features |
Hyperdiploid, highly rearranged with 21 clonal structural abnormalities, involving chromosomes 1, 2, 3, 4, 5, 7, 8, 9, 10, 11, 13, 14, 15, 16, 19, 20, some of them complex, losses of chromosomes 4, 18, 19, 21, 22; partial gain of 5, 11, some cells have double minutes.
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49(42-49), X, Y, 1x1, der(1)t(1;11)(q31-32;q13), der(1;15)(q10;q10), 2x2, der(2)t(2;3), 3x1, der(3)t(3;21)(p21;q ), 4x1, 5x2, i(5p), der(5?)t(2;5), der(5?)t(5q;7), 6x2, der(6)t(6;7), 7x1, der(7)del(7), 8x1, der(8)t(12;8;1), der(8)t(18;8;20), 9x1, der(9)t(9q;4;3), der(9)del(9), 10x1, der(10)t(3;10)(?;q24-25), der(10)del(10) a, 11x2, der(11)t(7;11)(?;q22-24), 12x1, der(13;14)(q10;q10)x2, 14x1, , 15x1, 16x2, 17x2, 18x1, 19x1, der(19)t(15;19), 20x1, der(20)t(5/16?;20), der(20)t(4;20), 21x1, 22x1, der(22)t(22;5;3), dmin a
a in less than 50% of cells
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