Table 2.

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

Indels, insertions and deletions; SNV, single nucleotide variant.