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GRCh37/hg19 11q22.3(chr11:106767102-107561488)x3 AND See cases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 16, 2014
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000511621.3

Allele description [Variation Report for GRCh37/hg19 11q22.3(chr11:106767102-107561488)x3]

GRCh37/hg19 11q22.3(chr11:106767102-107561488)x3

Genes:
CWF19L2:CWF19 like cell cycle control factor 2 [Gene - HGNC]
ELMOD1:ELMO domain containing 1 [Gene - OMIM - HGNC]
ALKBH8:alkB homolog 8, tRNA methyltransferase [Gene - OMIM - HGNC]
GUCY1A2:guanylate cyclase 1 soluble subunit alpha 2 [Gene - OMIM - HGNC]
Variant type:
copy number gain
Cytogenetic location:
11q22.3
Genomic location:
Chr11: 106767102 - 107561488 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 11q22.3(chr11:106767102-107561488)x3
HGVS:
    Links:
    dbVar: nssv13638801; dbVar: nsv2771426
    Observations:
    1

    Condition(s)

    Name:
    See cases [See the Variation display for details]
    Identifiers:

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    Assertion and evidence details

    Submission AccessionSubmitterReview Status
    (Assertion method)
    Clinical Significance
    (Last evaluated)
    OriginMethodCitations
    SCV000584802ISCA site 1

    See additional submitters

    no assertion criteria provided
    Uncertain significance
    (May 16, 2014)
    unknownclinical testing

    PubMed (1)
    [See all records that cite this PMID]

    Summary from all submissions

    EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
    humannot providedyes1not providednot providednot providednot providedclinical testing

    Citations

    PubMed

    Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

    Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RM, Lee C, Ostell JM, Rosenberg C, et al.

    Am J Hum Genet. 2010 May 14;86(5):749-64. doi: 10.1016/j.ajhg.2010.04.006. Review.

    PubMed [citation]
    PMID:
    20466091
    PMCID:
    PMC2869000

    Details of each submission

    From ISCA site 1, SCV000584802.1

    #EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
    1human1not providednot providedclinical testing PubMed (1)
    #SampleMethodObservation
    OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
    1unknownyesnot providednot providedDiscovery1not providednot providednot provided

    Last Updated: May 7, 2024