Variant DetailsVariant: nsv517343Internal ID | 15097950 | Landmark | | Location Information | | Cytoband | 3p26.3 | Allele length | Assembly | Allele length | hg38 | 579737 | hg19 | 579738 | hg18 | 579738 | hg17 | 579738 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv664739, nssv660938, nssv693695, nssv687451, nssv680980, nssv675641, nssv675545, nssv702191, nssv653211, nssv672083, nssv674906, nssv693169, nssv704994, nssv678732, nssv675797, nssv705320, nssv674568, nssv671856, nssv695189, nssv684338, nssv657747, nssv677924, nssv662329, nssv697376, nssv676753 | Samples | | Known Genes | CNTN6 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517343
| Frequency | Sample Size | 2026 | Observed Gain | 3 | Observed Loss | 31 | Observed Complex | 0 | Frequency | n/a |
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