Table 1.
CNV patterns in NSCLC patients (N = 1057).
| Gene | Diploid | Deep deletion | Shallow deletion | Copy number gain | Amplification | CNV sum | Percentage | |
|---|---|---|---|---|---|---|---|---|
| Eraser | ALKBH5 | 999 | 0 | 45 | 11 | 2 | 58 | 5.49 |
| FTO | 1004 | 2 | 30 | 20 | 1 | 53 | 5.01 | |
|
| ||||||||
| Writer | METTL14 | 1034 | 1 | 21 | 1 | 0 | 23 | 2.18 |
| METTL3 | 1032 | 1 | 20 | 1 | 3 | 25 | 2.37 | |
| WTAP | 1004 | 1 | 39 | 12 | 1 | 53 | 5.01 | |
|
| ||||||||
| Reader | YTHDF1 | 974 | 0 | 8 | 67 | 8 | 83 | 7.85 |
| YTHDF2 | 1027 | 0 | 24 | 6 | 0 | 30 | 2.84 | |
| YTHDC1 | 1039 | 0 | 12 | 1 | 5 | 18 | 1.70 | |
| YTHDC2 | 998 | 1 | 53 | 4 | 1 | 59 | 5.58 | |
| YTHDF3 | 964 | 0 | 6 | 81 | 6 | 93 | 8.80 | |
|
| ||||||||
| Others | EGFR | 915 | 4 | 12 | 82 | 44 | 142 | 13.43 |
| KRAS | 944 | 4 | 9 | 72 | 28 | 113 | 10.69 | |
| TP53 | 988 | 4 | 55 | 8 | 2 | 69 | 6.53 | |