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.
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD00010000594 |
SCOOP severe early-onset obesity cases
|
1720 |
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