Table 2. Number of genes affected by SCNA in seven melanoma cell lines.
CGH arrays | LAU-Me280 | LAU-Me246 | LAU-T618A | LAU-T50B | LAU-T149D | LAU-Me275 | LAU-Me235 | Unique gene count |
Deletion | 3668 | 4281 | 986 | 3656 | 108 | 122 | 1059 | 10711 |
Arm-level amplification | 222 | 0 | 549 | 99 | 998 | 42 | 0 | 1884 |
Focal amplification | 0 | 0 | 0 | 26 | 379 | 0 | 4 | 409 |
SNP arrays | LAU-Me280 | LAU-Me246 | LAU-T618A | LAU-T50B | LAU-T149D | LAU-Me275 | LAU-Me235 | Unique gene count |
Deletion | 2294 | 3157 | 2 | 113 | 70 | 2 | 39 | 5544 |
Arm-level amplification | 0 | 0 | 16584 | 1033 | 3477 | 16398 | 10384 | 19496 |
Focal amplification | 213 | 0 | 978 | 438 | 894 | 1853 | 161 | 4055 |
Number of genes affected by somatic deletions, arm-level amplifications (≥4 copies but <1 copy above the chromosome arm baseline) and focal amplifications (≥4 copies and ≥1 copy above the chromosome arm baseline), as measured using SNP or CGH arrays.