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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: 17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype

Fig. 3

Schematic overview of the 17p13.3 duplications previously reported and identified in our study (hg19). All the twenty-two blue blocks denote the previously reported duplicated regions. The lower red block denotes the identified duplication and the grey block denotes the identified triplication in our study. The complicated duplication found in our study contained a wider telocentric region than in previously reported 17p13.3 duplications

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