esv3626336
- Organism: Homo sapiens
- Study:estd214 (1000 Genomes Consortium Phase 3)
- Variant Type:copy number variation
- Method Type:Sequencing
- Submitted on:GRCh37
- Variant Calls:35
- Validation:Not tested
- Clinical Assertions: No
- Region Size:50,074
- Publication(s):1000 Genomes Project Consortium et al. 2015
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 673 SVs from 75 studies. See in: genome view
Overlapping variant regions from other studies: 726 SVs from 76 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3626336 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| esv3626336 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) |
Variant Call Information
| Variant Call ID | Type | Sample ID | Method | Analysis | Zygosity | Other Calls in this Sample and Study |
|---|---|---|---|---|---|---|
| essv14144814 | deletion | SAMN00630208 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,455 |
| essv14144815 | deletion | SAMN00630217 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,296 |
| essv14144816 | deletion | SAMN00630223 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,177 |
| essv14144817 | deletion | SAMN00630246 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,947 |
| essv14144818 | deletion | SAMN00779940 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,140 |
| essv14144819 | deletion | SAMN01036764 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,922 |
| essv14144820 | deletion | SAMN01090868 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,141 |
| essv14144821 | deletion | SAMN01090865 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,879 |
| essv14144822 | deletion | SAMN01036755 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,248 |
| essv14144823 | deletion | SAMN01090796 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,016 |
| essv14144824 | deletion | SAMN01036807 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,194 |
| essv14144825 | deletion | SAMN01090880 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,056 |
| essv14144826 | deletion | SAMN01090894 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,975 |
| essv14144827 | deletion | SAMN01090840 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,993 |
| essv14144828 | deletion | SAMN01090846 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,080 |
| essv14144829 | deletion | SAMN01090858 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,994 |
| essv14144830 | deletion | SAMN01090820 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,024 |
| essv14144831 | deletion | SAMN00001058 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,319 |
| essv14144832 | deletion | SAMN00000551 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,913 |
| essv14144833 | deletion | SAMN00001097 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,969 |
| essv14144834 | deletion | SAMN00001100 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,868 |
| essv14144835 | deletion | SAMN00001102 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,846 |
| essv14144836 | deletion | SAMN00001107 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,555 |
| essv14144837 | deletion | SAMN00001111 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,426 |
| essv14144838 | deletion | SAMN00001114 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,431 |
| essv14144839 | deletion | SAMN00001127 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,174 |
| essv14144840 | deletion | SAMN00001137 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,195 |
| essv14144841 | deletion | SAMN00001141 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,061 |
| essv14144842 | deletion | SAMN00001148 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,889 |
| essv14144843 | deletion | SAMN00001159 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,209 |
| essv14144844 | deletion | SAMN00001168 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,034 |
| essv14144845 | deletion | SAMN00001173 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,262 |
| essv14144846 | deletion | SAMN00001192 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,071 |
| essv14144847 | deletion | SAMN00007738 | Sequencing | Read depth and paired-end mapping | Heterozygous | 3,051 |
| essv14144848 | deletion | SAMN00004485 | Sequencing | Read depth and paired-end mapping | Heterozygous | 2,855 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Start | Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv14144814 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144815 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144816 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144817 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144818 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144819 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144820 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144821 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144822 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144823 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144824 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144825 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144826 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144827 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144828 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144829 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144830 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144831 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144832 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144833 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144834 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144835 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144836 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144837 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144838 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144839 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144840 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144841 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144842 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144843 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144844 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144845 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144846 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144847 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144848 | Remapped | Perfect | NC_000011.10:g.(50 406092_50407592)_( 50456665_50458165) del | GRCh38.p12 | First Pass | NC_000011.10 | Chr11 | 50,407,092 (-1000, +500) | 50,457,165 (-500, +1000) |
| essv14144814 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144815 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144816 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144817 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144818 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144819 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144820 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144821 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144822 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144823 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144824 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144825 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144826 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144827 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144828 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144829 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144830 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144831 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144832 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144833 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144834 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144835 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144836 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144837 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144838 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144839 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144840 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144841 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144842 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144843 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144844 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144845 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144846 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144847 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) | ||
| essv14144848 | Submitted genomic | NC_000011.9:g.(503 65263_50366763)_(5 0415836_50417336)d el | GRCh37 (hg19) | NC_000011.9 | Chr11 | 50,366,263 (-1000, +500) | 50,416,336 (-500, +1000) |