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Figure 2 | BMC Genomics

Figure 2

From: Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family

Figure 2

CNV detected by WES. CNV throughout the chromosomes – 1p13.3, 4q13.2, 5q35.3, 8p23.1, and 19q13.4 have distinct CNVs (14q32.3 is distinct, but contains variable regions associated with antibody production) (A), 8p23.1 containing beta-defensin clusters (B), and 1p13.1 containing GSTM1 (C) of eight subjects. Red and green dots are exons with p<0.05. Co-segregated regions of CNVs were also analyzed by Fisher’s exact test (D).

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BMC Genomics

ISSN: 1471-2164

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