Variant DetailsVariant: nsv515798Internal ID | 15096405 | Landmark | | Location Information | | Cytoband | 15q13.1 | Allele length | Assembly | Allele length | hg38 | 78077 | hg19 | 78077 | hg18 | 78077 | hg17 | 78077 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv697106, nssv676232, nssv669148, nssv685533, nssv679219, nssv677652, nssv682130, nssv673335, nssv655233, nssv691870, nssv699590, nssv657071, nssv674435, nssv657133, nssv688880, nssv697105, nssv685482, nssv655522, nssv680856, nssv674745, nssv664819, nssv677504, nssv667940, nssv685637, nssv676848, nssv667283, nssv689214 | Samples | | Known Genes | APBA2, FAM189A1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515798
| Frequency | Sample Size | 2026 | Observed Gain | 2 | Observed Loss | 25 | Observed Complex | 0 | Frequency | n/a |
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