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. 2020 Oct 2;11:540186. doi: 10.3389/fgene.2020.540186

TABLE 1.

The CNV patterns of m6A regulatory genes in HCC samples (n = 370).

Diploid Deep deletion Shallow deletion Copy number gain Amplification CNV sum Percentage
Writer METTL3 252 78 37 3 118 31.89%
METTL14 199 1 160 10 171 46.21%
METTL16 140 8 203 19 230 62.16%
WTAP 190 7 132 40 1 180 48.65%
KIAA1429 134 1 15 168 52 236 63.78%
ZC3H13 179 8 170 13 191 51.62%
RBM15 231 86 51 2 139 37.57%
Eraser ALKBH5 172 4 156 35 3 198 53.51%
FTO 202 4 143 21 168 45.41%
Reader YTHDF1 236 8 119 7 134 36.22%
YTHDF2 209 4 136 21 161 43.51%
YTHDF3 150 30 159 31 220 59.46%
YTHDC1 207 146 13 4 163 44.05%
YTHDC2 209 46 112 3 161 43.51%
IGF2BP1 234 27 102 7 136 36.76%
IGF2BP2 267 43 52 8 103 27.84%
IGF2BP3 233 16 116 5 137 37.03%
HNRNPA2B1 237 16 113 4 133 35.95%
HNRNPC 250 79 36 5 120 32.43%
TP53 132 9 216 13 238 64.32%

The CNV status was defined by GISTIC, including Deep deletion (homozygous deletion), Shallow deletion (heterozygous deletion), Diploid (normal copy number), Copy number gain (low level gain), and Amplification (high level amplification).