Number and type of genetic variants identified in purified BM MCs from SM patients by WGS (n = 4)
| Patient ID . | SNVs . | Indels . | Total variants (SNVs + indels) . | Mutations per Mb . |
|---|---|---|---|---|
| 9 | 15 | 7 | 22 | 0.008 |
| 10 | 486 | 15 | 501 | 0.18 |
| 13 | 534 | 21 | 555 | 0.19 |
| 14 | 267 | 9 | 276 | 0.10 |
| Average | 326 | 13 | 339 | 0.12 |
| Patient ID . | SNVs . | Indels . | Total variants (SNVs + indels) . | Mutations per Mb . |
|---|---|---|---|---|
| 9 | 15 | 7 | 22 | 0.008 |
| 10 | 486 | 15 | 501 | 0.18 |
| 13 | 534 | 21 | 555 | 0.19 |
| 14 | 267 | 9 | 276 | 0.10 |
| Average | 326 | 13 | 339 | 0.12 |
Indels, insertions and deletions; SNV, single nucleotide variant.