Journal of Genetic Medicine : eISSN 2383-8442 / pISSN 1226-1769

Fig. 1.

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Fig. 1. The classification of CNVs detected in 46 patients requested chromosomal microarray analysis. Possible clinical significance variants including pathogenic (P), likely pathogenic (LP), and variant of unknowns significance (VUS) were 27.0% (10/37) in symptomatic patients and 77.8% (7/9) in asymptomatic or pre-symptomatic patients. B, benign; LB, likely benign.
Journal of Genetic Medicine 2021;18:31-7
© 2021 Korean Society of Medical Genetics and Genomics