Description:
DUPLICATED CHROMOSOME
INVERTED CHROMOSOME
CHROMOSOME 15Q11-Q13 DUPLICATION SYNDROME
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Repository
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NIGMS Human Genetic Cell Repository
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| Subcollection |
Chromosome Abnormalities |
| Quantity |
25 µg |
| Quantitation Method |
Please see our FAQ |
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Biopsy Source
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Peripheral vein
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Cell Type
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B-Lymphocyte
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Tissue Type
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Blood
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Transformant
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Epstein-Barr Virus
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Sample Source
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DNA from LCL
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Race
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White
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Country of Origin
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USA
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Family History
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N
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Relation to Proband
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proband
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Confirmation
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Karyotypic analysis after cell line submission to CCR
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ISCN
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46,XX,inv(9)(p11q13),dup(15)(q11.2q13).arr 15q11.2q13.1(18906577-26757821)x3
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Species
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Homo sapiens
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Common Name
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Human
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Remarks
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| IDENTIFICATION OF SPECIES OF ORIGIN |
Species of Origin Confirmed by LINE assay |
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| Cytogenetics |
Chromosome 15: DUPLICATION Aneuploid Segment (+)15q11.2->15q12 |
| Remarks |
Clinically affected; examination at 11 years old reports: autism, ADOS calibrated severity score of 10, IQ of 89, normal EEG, round face, short bulbous nose, anteverted nares, long philtrum, full cheeks, diabetes mellitus, nasal labial folds assymmetry; 6.5 mb de novo 15q interstitial duplication of maternal origin; refer to patient 801-008 as described by Urraca et al PMID: 23495136. |
| Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013 |
| PubMed ID: 23665875 |
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| Urraca N, Cleary J, Brewer V, Pivnick EK, McVicar K, Thibert RL, Schanen NC, Esmer C, Lamport D, Reiter LT, The interstitial duplication 15q112-q13 syndrome includes autism, mild facial anomalies and a characteristic EEG signature Autism research : official journal of the International Society for Autism Research6:268-79 2012 |
| PubMed ID: 23495136 |
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