Fig. 1: Junction sequences for seven patients with DMD whole-exon deletions, aligned to the corresponding regions of the reference sequence NG_012232.1(DMD_v001).
From: Breakpoint junction features of seven DMD deletion mutations
Regions of microhomology are enclosed in boxes. Arrowheads indicate inferred breakpoint sites. New nucleotides are in bold type. Nonconsecutive direct repeats are underlined, with dashed and thicker lines used where necessary to distinguish complex repeat arrangements (d4). Left- and right-pointing arrows indicate the 5′ and 3′ spans, respectively, of short inverted repeats
