Variant DetailsVariant: nssv698528Internal ID | 15088494 | Landmark | | Location Information | | Cytoband | 20p11.1 | Allele length | Assembly | Allele length | hg38 | 2211539 | hg19 | 2211538 | hg18 | 2211538 | hg17 | 2211538 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv522873 | Supporting Variants | | Samples | | Known Genes | ABHD12, ACSS1, APMAP, CST7, ENTPD6, FAM182A, FAM182B, FLJ33581, GGTLC1, GINS1, LOC100134868, LOC284798, NANP, NCOR1P1, NINL, PYGB, SYNDIG1, VSX1, ZNF337 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nssv698528
| Frequency | Sample Size | 2026 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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