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. 2017 Apr 11;1:PO.16.00020. doi: 10.1200/PO.16.00020

Fig 2.

Fig 2

Total number of distinct genetic variants observed as patients were added to the clinical database. Because many variants are rare, new variants continue to be accumulated even after many patients have been sequenced. From these data, we estimate that the comparable ClinVar variants in this study (n = 2,006) correspond to the number that would be observed if approximately 22,000 patients had been tested by the same laboratories.