Variant DetailsVariant: esv2728854| Internal ID | 10312490 | | Landmark | | | Location Information | | | Cytoband | 4q35.1 | | Allele length | | Assembly | Allele length | | hg38 | 227 | | hg19 | 227 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6918391, essv6686944, essv6719064, essv6854677, essv6670553, essv6715164, essv6963098, essv6974126, essv6786033, essv6730539 | | Samples | SSM027, SSM087, SSM047, SSM069, SSM029, SSM017, SSM035, SSM031, SSM044, SSM043 | | 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) | esv2728854
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 10 | | Observed Complex | 0 | | Frequency | n/a |
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