Study

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity

Study ID Alternative Stable ID Type
EGAS00001000878 Other

Study Description

We performed SNP and copy number variation (CNV) association analyses in 1,509 children with obesity at the extreme tail (>3 s.d. from the mean) of the BMI distribution and 5,380 controls. The control samples were made available from the EGA with accession numbers EGAD00000000021 and EGAD00000000023.

Study Datasets 1 dataset.

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Dataset ID Description Technology Samples
EGAD00010000594
SCOOP severe early-onset obesity cases
1720

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