| Notable Features |
A hyperdiploid cell line with modal chromosome number of 47 and 9 structural translocations, one reciprocal translocation t(X;9) and one possible reciprocal translocation t(7;17) – the der(7) is observed in only two cells (the breakpoint is very terminal and could be misclassified); the der(17) is replaced by another der(17) t(7;17;4;11;3) in three cells which is a different clone and in these cells chr 2 has a translocated chr 17segment, which is not present in the first clone. The der(14?)t(14;13;8), is the same der(13)t(8;13), translocated as Rb fusion to chr 14. Gain of 5(q12-13- q ter).
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47(46-59). 1x2, 2x2, 3x2, 4x2, 5x2, del(5)(q11.2), 6x2, 7x2, 8x2, 9x1, der(9)t(X;9), 10x2, 11x2, 12x2, 13x1, der(13)t(8;13), der(?)t(14;13;8), 14x1, 15x2, 16x2, 17x1, der(17)t(7;17)(p22;?), 18x2, 19x2, 20x2, 21x2, 22x2, Xx1, der(X)t(X;9) cp[10]
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