estd220 (Pettigrew et al. 2015)
- Organism:
- Human
- Study Type:
- Case-Control
- Submitter:
- Kerry Pettigrew
- Description:
- We screened 86 children with language impairment and/or a family history of dyslexia for copy number variation (CNV). Participants were recruited as part of a longitudinal family study to investigate language and reading development in early childhood, and were assessed over a period of approximately 5 years. DNA was genotyped on an Illumina Human OmniExpress-24 platform, and CNVs predicted using QuantiSNP and PennCNV. Reported CNVs span at least three consecutive genetic variants, have a confidence score > 10, and were predicted by both algorithms. See Variant Summary counts for estd220 in dbVar Variant Summary.
- Publication(s):
- Pettigrew et al. 2015