Variant DetailsVariant: nsv515519Internal ID | 15096126 | Landmark | | Location Information | | Cytoband | 9q21.11 | Allele length | Assembly | Allele length | hg38 | 27550 | hg19 | 27550 | hg18 | 27550 | hg17 | 27550 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv679148, nssv658314, nssv664193, nssv686124, nssv651809, nssv657632, nssv693526, nssv672478, nssv681182, nssv655439, nssv677635, nssv661864, nssv678641, nssv655725, nssv691788, nssv671411, nssv666088 | Samples | | Known Genes | APBA1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515519
| Frequency | Sample Size | 2026 | Observed Gain | 5 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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