Variant DetailsVariant: esv2722045| Internal ID | 10305681 | | Landmark | | | Location Information | | | Cytoband | 20p13 | | Allele length | | Assembly | Allele length | | hg38 | 536 | | hg19 | 536 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv646e201 | | Supporting Variants | essv6747434, essv6902094, essv6771486, essv6666172, essv6901261, essv6741777 | | Samples | SSM100, SSM029, SSM001, SSM055, SSM052, SSM012 | | 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) | esv2722045
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 6 | | Observed Complex | 0 | | Frequency | n/a |
|
|