Variant DetailsVariant: nsv517423Internal ID | 15098030 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 720587 | hg19 | 720587 | hg18 | 720587 | hg17 | 720587 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv696846, nssv657841, nssv655808, nssv679296, nssv660015, nssv696217, nssv660932, nssv655664, nssv651980, nssv703026, nssv664310, nssv681994, nssv680227, nssv665223 | Samples | | Known Genes | ASIC2, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517423
| Frequency | Sample Size | 2026 | Observed Gain | 2 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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