Variant DetailsVariant: esv2728142Internal ID | 9962455 | Landmark | | Location Information | | Cytoband | 4q25 | Allele length | Assembly | Allele length | hg38 | 183 | hg19 | 183 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6690048, essv6781779, essv6813944, essv6722840, essv6711447, essv6777752, essv6951466, essv6848415, essv6726715 | Samples | SSM036, SSM045, SSM046, SSM042, SSM067, SSM086, SSM068, SSM077, SSM025 | Known Genes | | 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) | esv2728142
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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