Variant DetailsVariant: nssv534851Internal ID | 15157754 | Landmark | | Location Information | | Cytoband | 17q11.2 | Allele length | Assembly | Allele length | hg38 | 397403 | hg19 | 397403 | hg18 | 397403 | hg17 | 397403 |
| Variant Type | CNV loss | Copy Number | 1 | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv457720 | Supporting Variants | | Samples | 1782681208_A | Known Genes | ADAP2, ATAD5, CRLF3, DPRXP4, LRRC37BP1, RNF135, SH3GL1P2, SUZ12P1, TEFM | Method | SNP array | Analysis | An HMM examining LogR Ratio and B-allele Frequency was used to classify SNP array data into regions of copy-number 0-3. A combination of manual and automated curation was used on the resulting output to reduce false positives. | Platform | Not reported | Comments | | Reference | Itsara_et_al_2009 | Pubmed ID | 19166990 | Accession Number(s) | nssv534851
| Frequency | Sample Size | 1557 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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