Variant DetailsVariant: esv2733115Internal ID | 9967437 | Landmark | | Location Information | | Cytoband | 6q26 | Allele length | Assembly | Allele length | hg38 | 434 | hg19 | 434 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1032e201 | Supporting Variants | essv6676704, essv6719572, essv6730999, essv6715660, essv6774699, essv6845072, essv6698021, essv6889088 | Samples | SSM038, SSM047, SSM032, SSM044, SSM066, SSM085, SSM043, SSM012 | Known Genes | PACRG-AS1 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2733115
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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