Variant DetailsVariant: esv2731356Internal ID | 9965673 | Landmark | | Location Information | | Cytoband | 6p25.3 | Allele length | Assembly | Allele length | hg38 | 570 | hg19 | 570 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6830072, essv6872635, essv6793965, essv6739875, essv6767418, essv6690319, essv6778071, essv6886924, essv6822352, essv6963539, essv6907419, essv6848950 | Samples | SSM036, SSM027, SSM064, SSM079, SSM009, SSM096, SSM067, SSM014, SSM086, SSM081, SSM091, SSM052 | Known Genes | EXOC2 | 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) | esv2731356
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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