Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants
Article first published online: 14 MAR 2011
© 2011 The Authors Annals of Human Genetics © 2011 Blackwell Publishing Ltd/University College London
Annals of Human Genetics
Special Issue: Annals Online Archive 1925-1954
Volume 75, Issue 3, pages 383–397, May 2011
How to Cite
Fernando, M. M. A., de Smith, A. J., Coin, L., Morris, D. L., Froguel, P., Mangion, J., Blakemore, A. I. F., Graham, R. R., Behrens, T. W. and Vyse, T. J. (2011), Investigation of the HIN200 Locus in UK SLE Families Identifies Novel Copy Number Variants. Annals of Human Genetics, 75: 383–397. doi: 10.1111/j.1469-1809.2011.00641.x
- Issue published online: 13 APR 2011
- Article first published online: 14 MAR 2011
- Received: 3 September 2010, Accepted: 21 December 2010
Figure S1 Consensus sequence for region surrounding SNPs, rs856089 and rs856142.
Table S1 Quality control information for all 86 SNPs put forward for genotyping at the HIN200 locus in UK SLE trios.
Table S2 Single marker association analysis for 52 SNPs across the HIN200 locus in a European-American SLE case–control cohort.
Table S3 HIN200 sequencing primers for SNPs rs856089 and rs856142.
Table S4 Comparison of copy number variation events (CNVEs) identified by The Copy Number Variation Discovery Project across the HIN200 region in three HapMap populations.
Table S5 Subphenotype association analysis across the HIN200 locus in UK SLE trios.
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