nstd155 (Adewoye et al. 2018)
- Organism:
- Human
- Study Type:
- Control Set
- Submitter:
- Edward Hollox
- Description:
- In this study we use high-coverage phase 3 exome sequences of the 1000 Genomes project to infer diploid copy number of the CCL3L1 genomic region, a well-studied CNV that carries CCL3L1 and CCL4L1. We use the sequence read depth approach to measure copy number, using the CNVrd2 software. See Variant Summary counts for nstd155 in dbVar Variant Summary.
- Publication(s):
- Adewoye et al. 2018