Fig. 6From: A rare cardiac phenotype of dextrocardia observed in a fetus with 1p36 deletion syndrome and a balanced translocation: a prenatal case reportIntegrative Genomics Viewer (IGV) screenshot of whole genome sequencing pair-end reads of the fetus. The dashed lines indicate the breakpoints on chromosomes 5 and 6. Junctions reads sequence are shown belowBack to article page