Variant DetailsVariant: nsv517066 Internal ID | 15097673 | Landmark | | Location Information | | Cytoband | 12q13.13 | Allele length | Assembly | Allele length | hg38 | 334329 | hg19 | 334329 | hg18 | 334329 | hg17 | 334329 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv689893, nssv692890, nssv653279, nssv655026, nssv663755, nssv655358, nssv663667, nssv674334, nssv669794, nssv670606, nssv652339, nssv657807, nssv674194, nssv652857, nssv661533, nssv681824, nssv699709, nssv661140, nssv683336, nssv691076, nssv693629, nssv670952, nssv682223, nssv658412, nssv662487, nssv653723, nssv667423, nssv675597, nssv657233, nssv693430, nssv657491, nssv679753, nssv684821, nssv665557, nssv694517, nssv691972, nssv692446, nssv668331, nssv687149, nssv660173, nssv692422, nssv672368, nssv677764, nssv667936, nssv677722, nssv666122, nssv703541, nssv669550, nssv672758 | Samples | | Known Genes | AAAS, C12orf10, CSAD, EIF4B, ESPL1, IGFBP6, ITGB7, LOC283335, MFSD5, MIR6757, PFDN5, RARG, SOAT2, SP7, SPRYD3, TENC1, ZNF740 | Method | SNP array | Analysis | Sample-level CNVs | Platform | GPL6434 | Comments | | Reference | Shaikh_et_al_2009 | Pubmed ID | 19592680 | Accession Number(s) | nsv517066
| Frequency | Sample Size | 2026 | Observed Gain | 0 | Observed Loss | 49 | Observed Complex | 0 | Frequency | n/a |
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