Frequency of aCGH copy number aberrations associated with poor prognosis among the H-MM subtype
| Aberration . | Frequency AA patients, % (n) . | Frequency EA patients, % (n) . | P value (Fisher’s) . | Corrected P value . |
|---|---|---|---|---|
| 1p deletion | 63 (15/24) | 50 (52/103) | .366 | .999 |
| p18 deletion | 46 (11/24) | 31 (32/103) | .231 | .977 |
| p18 homozygous deletion | 0 (0/24) | 5 (5/103) | .583 | .999 |
| 1q gain | 29 (7/24) | 60 (62/103) | .007 | .083 |
| 8p deletion | 67 (16/24) | 57 (59/103) | .492 | .999 |
| 13q deletion | 33 (8/24) | 31 (32/103) | 1 | 1 |
| 13 monosomy | 25 (6/24) | 17 (18/103) | .564 | .999 |
| 14q deletion | 33 (8/24) | 32 (33/103) | 1 | 1 |
| 16q deletion | 25 (6/24) | 39 (40/103) | .244 | .977 |
| 17p deletion | 8 (2/24) | 10 (10/103) | 1 | 1 |
| 22q deletion | 21 (5/24) | 22 (23/103) | 1 | 1 |
| Aberration . | Frequency AA patients, % (n) . | Frequency EA patients, % (n) . | P value (Fisher’s) . | Corrected P value . |
|---|---|---|---|---|
| 1p deletion | 63 (15/24) | 50 (52/103) | .366 | .999 |
| p18 deletion | 46 (11/24) | 31 (32/103) | .231 | .977 |
| p18 homozygous deletion | 0 (0/24) | 5 (5/103) | .583 | .999 |
| 1q gain | 29 (7/24) | 60 (62/103) | .007 | .083 |
| 8p deletion | 67 (16/24) | 57 (59/103) | .492 | .999 |
| 13q deletion | 33 (8/24) | 31 (32/103) | 1 | 1 |
| 13 monosomy | 25 (6/24) | 17 (18/103) | .564 | .999 |
| 14q deletion | 33 (8/24) | 32 (33/103) | 1 | 1 |
| 16q deletion | 25 (6/24) | 39 (40/103) | .244 | .977 |
| 17p deletion | 8 (2/24) | 10 (10/103) | 1 | 1 |
| 22q deletion | 21 (5/24) | 22 (23/103) | 1 | 1 |