Table 1.

Variant counts identified in bulk tumor population and SC exomes

Variants called*Nonsynonymous SNVSynonymous SNVStopgain SNVFrameshift insertionFrameshift deletionTotal
Bulk tumor exome 20 14 48 
 In 1 or more SCs 16 10 34 
 Not in 1 or more SCs 14 
Total in 2 or more SCs 28 16 51 
 In bulk tumor 16 30 
 Not in bulk tumor 12 21 
Total unique variants 32 21 10 69 
Variants called*Nonsynonymous SNVSynonymous SNVStopgain SNVFrameshift insertionFrameshift deletionTotal
Bulk tumor exome 20 14 48 
 In 1 or more SCs 16 10 34 
 Not in 1 or more SCs 14 
Total in 2 or more SCs 28 16 51 
 In bulk tumor 16 30 
 Not in bulk tumor 12 21 
Total unique variants 32 21 10 69 

SNV, single-nucleotide variant.

*

Variant counts of each type are tabulated for the bulk tumor and SC exomes. For the SC exomes, selection criteria required that the variant be present in 2 or more SC cells to be counted. The number of variants identified in 2 or more SC exomes that were also called (n = 30) or not called (n = 21) in the bulk tumor exome are also given.

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