nstd101 (obsolete - ClinGen Kaminsky et al. 2011)
- Organism:
- Human
- Study Type:
- Case-Set
- Submitter:
- Multiple clinical cytogenetics laboratories, as described in Kaminsky et al. 2011
- Submitter URL:
- http://www.clinicalgenome.org
- Description:
- Copy number variation identified through the course of routine clinical cytogenomic testing in postnatal populations. Clinical assertions have been curated as described in Kaminsky, et al. 2011. For additional ClinGen data, please see nstd37. See Variant Summary counts for nstd101 in dbVar Variant Summary.
- Curatorial Comment:
- PLEASE NOTE: Replaced nstd101 variant regions with variants in [nstd102|/dbvar/studies/nstd102]
- Project:
- PRJNA42509
- Publication(s):
- Kaminsky et al. 2011
- dbGaP Release Date:
- 2016-06-20
- Last updated:
- 2017-07-07
- Date Obsoleted:
- 2021-11-03
- Replacement Study:
- nstd102