Skip to main content
Fig. 2 | BMC Medical Genomics

Fig. 2

From: Identification of two novel large deletions in FBN1 gene by next-generation sequencing and multiplex ligation-dependent probe amplification

Fig. 2

CNV detection by NGS. Read depth (coverage tracks) of 60× PE150 PCR-free WGS data for Patient 1 and a control for the deleted and flanking genomic regions displayed in IGV. CNV, copy number variation; NGS, next-generation sequencing; WGS, whole-genome sequencing; IGV, Integrative Genomics Viewer [http://www.broadinstitute.org/igv/, accessed Dec 2016]

Back to article page

BMC Medical Genomics

ISSN: 1755-8794

Contact us