Skip to main content
Figure 1 | BMC Genomics

Figure 1

From: A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies

Figure 1

DMD-CGH array profiles of deletions and duplications in patients with known mutations, identified by MLPA. a) case 1, duplication of exon 2; b) case 2, deletion of exon 14; c) case 3, duplication of exons 3–6; d) case 4, duplication of exons 65–79. In figure 1a and c the intron 2 CNV is visible around 32.9 Mb.

Back to article page