Variant DetailsVariant: nsv515747Internal ID | 15096354 | Landmark | | Location Information | | Cytoband | 9p24.2 | Allele length | Assembly | Allele length | hg38 | 1084 | hg19 | 1084 | hg18 | 1084 | hg17 | 1084 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv667457, nssv678526, nssv674041, nssv664665, nssv671317, nssv669880, nssv660317, nssv676226, nssv675805, nssv673699, nssv684727, nssv685859, nssv691930 | Samples | | Known Genes | SLC1A1 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515747
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
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