nstd37 (obsolete - ClinGen Laboratory-Submitted)
- Organism:
- Human
- Study Type:
- Case-Set
- Submitter:
- Multiple clinical cytogenetics laboratories, through the ClinGen Resource
- Submitter URL:
- http://www.clinicalgenome.org
- Description:
- Copy number variation identified through the course of routine clinical cytogenomic testing in postnatal populations, with clinical assertions as classified by the original submitter. For data from the original published study, Kaminsky, et al. 2011, please see nstd101. See Variant Summary counts for nstd37 in dbVar Variant Summary.
- Curatorial Comment:
- PLEASE NOTE: Replaced nstd37 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Project:
- PRJNA42509
- Publication(s):
- Miller et al. 2010
- dbGaP Release Date:
- 2016-06-20
- Last updated:
- 2017-07-08
- Date Obsoleted:
- 2021-11-17
- Replacement Study:
- nstd102