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. Author manuscript; available in PMC: 2013 Feb 19.
Published in final edited form as: Ann Hum Genet. 2012 Mar 2;76(3):211–220. doi: 10.1111/j.1469-1809.2012.00704.x

Figure 2A. Initial evidence in whole exome sequencing of a 3 basepair deletion in RSPH9.

Figure 2A

A single molecular read (upper panel) showing a deletion was observed (horizontal thin line adjacent to thedotted lines flanking the base centred in the viewing panel). Compared with a control (lower panel), there was also a deficiency of mapped reads at this location. The wildtype sequence shows a microrepeat 5′-GAAGAA.