A Genome-Wide Assessment of the Role of Untagged Copy Number Variants in Type 1 Diabetes
Figure 1
Summary of the CNVs included in the array design and tested for T1D association using FBAT-CNV.
CNVs originate from two main sources: the GSV map of common CNVs [27] and the 1,000 Genomes sequence data. Tested CNVs also include 365 novel insertion CNVs obtained from the Venter genome. Detailed description of the array design is provided in Text S1.