The American Journal of Human Genetics, Volume 82, Issue 3, 685-695 3 March 2008

doi:10.1016/j.ajhg.2007.12.010

The Fine-Scale and Complex Architecture of Human Copy-Number Variation

Supplemental Data for Perry et al.

Document S1. Five Figures (PDF 462 kb)
Document S2. Depictions of Individual Mean Log2 Ratios for 236 Discretely Clustering CNVs (PDF 1705 kb)
Document S3. Heatmap Depictions of 101 Complex CNV Regions (PDF 2390 kb)
Table S1. Sample-Level CNV Calls for 30 HapMap Individuals, Using All Genome-Wide Perfect Match Probes (PDF 2324 kb)
Table S2. Sample-Level CNV Calls for 30 HapMap Individuals, Using the Proximal Probe Set (XLS 2957 kb)
Table S3. CNV Regions and Comparison to Previous Studies (XLS 903 kb)
Table S4. CNV Regions in the Database of Genomic Variants, Compared to CNV Regions in this Study (XLS 238 kb)
Table S5. Comparison of Sample-Level CNV Calls between Redon et al. Study and This Study (XLS 615 kb)
Table S6. Summary of Sample-Level Comparison between Redon et al. Study and This Study (XLS 24 kb)
Table S7. Concordance in Sample-Level CNV Calls between This Study and Redon et al. Study, for all 270 HapMap Individuals (XLS 325 kb)
Table S8. Summary of Sequenced Deletion CNV Breakpoints and PCR Primers for All Attempted Regions (XLS 44 kb)
Table S9. CNVs Containing Probes with Perfect Matches to Other CNVs in the Genome (XLS 105 kb)
Table S10. Complex CNV Regions (XLS 66 kb)
Table S11. Complex CNV Region qPCR Primers and Results (XLS 43 kb)

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