Table 2. Frequency of Molecular Aberrations.
No. of patients | % | |
---|---|---|
# of patients consented for molecular analysis | 428 | 100 |
# of specimens quality control passed | 407 | |
No. of aberrations detected for AmpliSeq | ||
0 | 65 | 15.9 |
1 | 141 | 34.6 |
2 | 123 | 30.2 |
3 | 51 | 12.5 |
≥4 | 27 | 6.6 |
No. of patients with at least one aberrations by AmpliSeq alone | 342 | 84.1 |
# of specimens available for both Ampliseq and 21-gene copy number variation array | 281 | |
No. of aberrations detected for AmpliSeq and 21-gene copy number variation array* | ||
0 | 41 | 14.6 |
1 | 79 | 28.1 |
2 | 81 | 28.8 |
3 | 51 | 18.1 |
≥4 | 29 | 10.3 |
N = 407 Ampliseq 2.0 + 21-gene copy number variation array; N = 281, Ampliseq 2.0 available