Open Access Research article

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

Linlu Zhao1, Elizabeth W Triche2, Kyle M Walsh1, Michael B Bracken1, Audrey F Saftlas3, Josephine Hoh4 and Andrew T Dewan15*

Author Affiliations

1 Center for Perinatal, Pediatric and Environmental Epidemiology, Yale School of Public Health, New Haven, CT, USA

2 Department of Epidemiology, Brown University School of Medicine, Providence, RI, USA

3 Department of Epidemiology, University of Iowa College of Public Health, Iowa City, IA, USA

4 Division of Environmental Health Sciences, Yale School of Public Health, New Haven, CT, USA

5 Division of Chronic Disease Epidemiology, Yale School of Public Health, 60 College Street, Room 403, New Haven, CT, 06520, USA

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BMC Pregnancy and Childbirth 2012, 12:61  doi:10.1186/1471-2393-12-61

Published: 29 June 2012

Additional files

Additional file 1:

Table S1.SNP genotyping data quality. SNP genotyping data quality summary.

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Additional file 2:

Table S2.Regions of autosomal copy-number deletion meeting initial prioritization criteria. Annotated list of autosomal deletions enriched among cases that met initial prioritization criteria.

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Additional file 3:

Table S3.Regions of autosomal copy-number amplification meeting initial prioritization criteria. Annotated list of autosomal amplifications enriched among cases that met initial prioritization criteria.

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Additional file 4:

Table S4.X chromosome CNV regions meeting initial prioritization criteria. Annotated list of candidate CNV regions in X chromosome enriched among cases that met initial prioritization criteria.

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