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. 2015 Oct;1(1):a000422. doi: 10.1101/mcs.a000422

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© 2015 Jiménez-Barrón et al.; Published by Cold Spring Harbor Laboratory Press

This article is distributed under the terms of the Creative Commons Attribution-NonCommercial License, which permits reuse and redistribution, except for commercial purposes, provided that the original author and source are credited.

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Figure 7. — Genome Browser Screen view for the read depths in the SSC_12596 CNV 4p16.3 region of 50 kb. The highlighted region is where the four people bear either a homozygous or heterozygous deletion, only the proband has a homozygous deletion including the highlighted area plus the two regions indicated by the red arrows, which could have been generated by inheriting the deleted copy from both parents.