Variant DetailsVariant: nsv615190Internal ID | 16055913 | Landmark | | Location Information | | Cytoband | 9q31.3 | Allele length | Assembly | Allele length | hg38 | 675 | hg19 | 675 | hg18 | 675 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1141234, nssv1141233, nssv1141236, nssv1141235, nssv1141237, nssv1141238 | Samples | | Known Genes | KIAA0368 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nsv615190
| Frequency | Sample Size | 17421 | Observed Gain | 5 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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