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. 2015 Mar 17;16:14. doi: 10.1186/s12881-015-0162-5

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© Imtiaz et al.; licensee BioMed Central. 2015

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Detailed AutoSNPa homozygosity mapping analysis for all chromosomes in 12 family members. The four shared ROH’s in the affected sisters are indicated by red boxes, whose coordinates are detailed in the table. The arrows point to the unaffected individuals that cancel out three of the ROHs on chromosomes 1 and 4. In addition, narrowing of the remaining ROH on chromosome 3 containing DNAH1 is indicated by red arrows due to shared region present in 2 unaffected siblings (III:3 and III:5).