Table 1.
Set 1 | Set 2 | Set 3 | Set 4 | |
---|---|---|---|---|
Mutation types | SNV, structural variation (SV) (deletions, duplications, inversions) | SNV, SV (deletions, duplications, insertions, inversions) | SNV, SV (deletions, duplications, insertions, inversions) & INDEL | SNV, SV (deletions, duplications, inversions) & INDEL |
Number of Somatic SNVs | 3535 | 4322 | 7903 | 16,268 |
Cellularity | 100% | 80% | 100% | 80% |
Subclone variant allele frequencies (VAFs) | N/A | N/A | 50%, 33%, 20% | 50%, 35% (effectively 30% and 15% due to cellularity) |