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Fig. 2 | BMC Medical Genomics

Fig. 2

From: A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature

Fig. 2

Schematic representation of chromosome region 15q25.2 using UCSC Genome Browser assembly February 2009 hg19. The missing areas in our patient were 15q25.2 83,588,055-84,035,418 when compared to female patients who were reported to have lost the same area. The minimum deleted area in each patient is indicated by a solid black bar and the largest deleted area is indicated in red color. The yellow area represents the missing area in this patient

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