Frequency of copy number aberrations associated with poor prognosis among the NH-MM subtype
| Aberration . | Frequency AA patients, % (n) . | Frequency EA patients, % (n) . | P value (Fisher’s) . | Corrected P value . |
|---|---|---|---|---|
| 1p deletion | 52 (11/21) | 51 (47/93) | 1 | 1 |
| p18 deletion | 33 (7/21) | 24 (22/93) | .586 | .879 |
| p18 homozygous deletion | 10 (2/21) | 1 (1/93) | .093 | .315 |
| 1q gain | 38 (8/21) | 52 (48/93) | .240 | .480 |
| 8p deletion | 29 (6/21) | 32 (30/93) | .800 | .960 |
| 13q deletion | 48 (10/21) | 62 (58/93) | .157 | .378 |
| 13 monosomy | 33 (7/21) | 52 (48/93) | .104 | .312 |
| 14q deletion | 24 (5/21) | 56 (52/93) | .008 | .097 |
| 16q deletion | 43 (9/21) | 39 (36/93) | 1 | 1 |
| 17p deletion | 0 (0/21) | 16 (15/93) | .071 | .312 |
| 22q deletion | 19 (4/21) | 30 (28/93) | .304 | .521 |
| Aberration . | Frequency AA patients, % (n) . | Frequency EA patients, % (n) . | P value (Fisher’s) . | Corrected P value . |
|---|---|---|---|---|
| 1p deletion | 52 (11/21) | 51 (47/93) | 1 | 1 |
| p18 deletion | 33 (7/21) | 24 (22/93) | .586 | .879 |
| p18 homozygous deletion | 10 (2/21) | 1 (1/93) | .093 | .315 |
| 1q gain | 38 (8/21) | 52 (48/93) | .240 | .480 |
| 8p deletion | 29 (6/21) | 32 (30/93) | .800 | .960 |
| 13q deletion | 48 (10/21) | 62 (58/93) | .157 | .378 |
| 13 monosomy | 33 (7/21) | 52 (48/93) | .104 | .312 |
| 14q deletion | 24 (5/21) | 56 (52/93) | .008 | .097 |
| 16q deletion | 43 (9/21) | 39 (36/93) | 1 | 1 |
| 17p deletion | 0 (0/21) | 16 (15/93) | .071 | .312 |
| 22q deletion | 19 (4/21) | 30 (28/93) | .304 | .521 |