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Figure 3 | BMC Pregnancy and Childbirth

Figure 3

From: Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients

Figure 3

UCSC Genome Browser plot of the PSG gene family region (chr19:47.918-48.465 Mb). (A) Each red horizontal bar represents the length and breakpoints of a putative deletion called in PE cases or controls. (B) UCSC Genes located within this region. Asterisks indicate the genomic positions of nominally significant SNPs (from left to right: rs4030933, rs2159027, rs10417319, and rs10402173). (C) Segmental duplications of ≥1 kb with 90-98% sequence similarity.

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