GRCh37/hg19 16p13.11-12.3(chr16:15489453-18321582)x1 AND 16p13.11 microdeletion syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003329551.1
Allele description [Variation Report for GRCh37/hg19 16p13.11-12.3(chr16:15489453-18321582)x1]
GRCh37/hg19 16p13.11-12.3(chr16:15489453-18321582)x1
Condition(s)
- Name:
- 16p13.11 microdeletion syndrome
- Identifiers:
- MONDO: MONDO:0016836; MedGen: C4304596
Assertion and evidence details
Last Updated: Sep 30, 2023