Variant DetailsVariant: nsv515568Internal ID | 15096175 | Landmark | | Location Information | | Cytoband | 6q27 | Allele length | Assembly | Allele length | hg38 | 291520 | hg19 | 291520 | hg18 | 291520 | hg17 | 291520 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv676241, nssv701335, nssv655977, nssv688132, nssv668141, nssv682244, nssv664114, nssv679985, nssv674061, nssv671628, nssv654873, nssv670545, nssv663929, nssv701625, nssv666706, nssv666881, nssv666637, nssv678176, nssv693442, nssv700319, nssv689118, nssv681569, nssv667552, nssv694840, nssv696820, nssv667298, nssv669582, nssv685952 | Samples | | Known Genes | FRMD1, HGC6.3, KIF25, KIF25-AS1, MLLT4 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv515568
| Frequency | Sample Size | 2026 | Observed Gain | 19 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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