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

Fig. 1.

Download original image
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 https://doi.org/10.5734/JGM.2021.18.1.31
© 2021 Korean Society of Medical Genetics and Genomics