Variant DetailsVariant: esv2734406Internal ID | 9968733 | Landmark | | Location Information | | Cytoband | 10p12.1 | Allele length | Assembly | Allele length | hg38 | 3301 | hg19 | 3301 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6768943, essv6775410, essv6896198, essv6832532, essv6763183, essv6803256, essv6935767, essv6791512, essv6752328, essv6845693, essv6906362, essv6668042, essv6709109, essv6897402, essv6976533, essv6842128, essv6965237, essv6724179, essv6737653, essv6681282, essv6677502, essv6720368, essv6743782 | Samples | SSM008, SSM027, SSM045, SSM073, SSM050, SSM002, SSM057, SSM084, SSM021, SSM029, SSM062, SSM032, SSM044, SSM033, SSM066, SSM006, SSM085, SSM053, SSM010, SSM070, SSM099, SSM030, SSM012 | Known Genes | PDSS1 | 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) | esv2734406
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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