Variant DetailsVariant: nsv515548Internal ID | 15096155 | Landmark | | Location Information | | Cytoband | 10p11.23 | Allele length | Assembly | Allele length | hg38 | 15238 | hg19 | 15238 | hg18 | 15238 | hg17 | 15238 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv692794, nssv681776, nssv671218, nssv675278, nssv689015, nssv664059, nssv687437, nssv667241, nssv677353, nssv693090, nssv671042, nssv655380, nssv675537, nssv663877, nssv689794, nssv669862, nssv686096 | Samples | | Known Genes | MIR8086, MPP7 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515548
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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