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Fig. 1 | Human Genomics

Fig. 1

From: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

Fig. 1

XHMM plots for copy number variations (CNV): CNV deletion region for chr6:109466479-109485174. x-axis represents the genome locus, and y-axis is the computed Z-score of PCA normalized read depth; positive values indicate duplication and negative values indicate deletion; target individuals are highlighted with color while gray lines are the control individuals from 663 population pool

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Human Genomics

ISSN: 1479-7364