TABLE 1.
Founder line | No. tumors karyotyped | Recurrent rearrangements | Other recurrent alterations |
---|---|---|---|
42 | 15 | inv(6)(A2B1) [15]* | +14 [6], +15 [12], +16 [3] |
54 | 2 | t(14;15)(C2;D1) [2] | +10 [1], +14 [1], +der(14)t(14;15) [1], +15 [1], +der(15)t(14;15) [2] |
55 | 7 | inv(6)(A2B1) [1] t(14;15)(C2;D1) [4] | +10 [3], +14 [1], +der(14)t(14;15) [1], +15 [2], +der(15)t(14;15) [4], +16 [2] |
62 | 5 | t(14;15)(C2;D1) [2] | +10 [1], +14 [2], +der(14)t(14;15) [1], +15 [3], +der(15)t(14;15) [2], +16 [2] |
72 | 5 | t(14;15)(C2;D1) [5] | +10 [3], +14 [1], +der(14)t(14;15) [2], +der(15)t(14;15) [5] |
79 | 3 | inv(6)(A2B1) [1] t(14;15)(C2;D1) [1] | +10 [1], +14 [1], +15 [2], +der(15)t(14;15) [1] |
Numbers in brackets indicate number of tumors showing given chromosomal alteration.