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Fig. 2 | BMC Medical Genomics

Fig. 2

From: The diagnostic yield of intellectual disability: combined whole genome low-coverage sequencing and medical exome sequencing

Fig. 2

Map of CNVs associated with varying phenotypes of known genomic disorders. a) Two concurrent pathogenic CNVs, 2q37.1-q37.3 deletion and 19q13.42-q13.43 duplication, in patient 12. b) Two concurrent pathogenic CNVs, 2q37.3 deletion and 20p12.1-p13 duplication, in patient 13. c) Map of 2q37 deletions with included genes in 2 patients. and d) Map of 17q12 deletions with included genes in patient 9

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