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. Author manuscript; available in PMC: 2013 Dec 1.

Published in final edited form as: Am J Med Genet A. 2012 Nov 19;158A(12):3137–3147. doi: 10.1002/ajmg.a.35664

a and c: a total of 91 pair-wise combinations were evaluated for shared segments across the entire genome (7 isolated CDH patients, total of 14 haplotypes). Results for chromosome 8 (a) and 15 (c) are plotted along HapMap centimorgan (cM) recombination maps. The maximum number of consecutive inclusion markers across each chromosome is shown at the bottom of the plot and depicted as the height of a segment along the Y axis. b and d: the shared haplotypes were compared against paternal and maternal haplotypes from 24 children who did not have CDH (total of 48 haplotypes) to eliminate the possibility of common haplotypes. Neither the chromosome 8 (b) or 15 (d) shared segment was found to be a common haplotype.

a and c: a total of 91 pair-wise combinations were evaluated for shared segments across the entire genome (7 isolated CDH patients, total of 14 haplotypes). Results for chromosome 8 (a) and 15 (c) are plotted along HapMap centimorgan (cM) recombination maps. The maximum number of consecutive inclusion markers across each chromosome is shown at the bottom of the plot and depicted as the height of a segment along the Y axis. b and d: the shared haplotypes were compared against paternal and maternal haplotypes from 24 children who did not have CDH (total of 48 haplotypes) to eliminate the possibility of common haplotypes. Neither the chromosome 8 (b) or 15 (d) shared segment was found to be a common haplotype.