| identifier | PRJEB11771 | ||
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| type | bioproject | ||
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| title | Targeted resequencing of the remaining allele in the 22q11 region for 127 patients | ||
| description | The 22q11.2 deletion syndrome is the most common microdeletion disorder, with wide phenotypic variability. To investigate variation within the non-deleted allele we performed targeted Illumina HiSeq 2000 resequencing of the 22q11.2 region for 127 patients, identifying multiple deletion sizes, and approximately 12 thousand hemizygous variant positions. | ||
| data type | Other | ||
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| distribution | JSONJSON-LD | ||
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| status | public | ||
| visibility | unrestricted-access | ||
| dateCreated | 2015-12-18T00:00:00Z | ||
| dateModified | 2015-12-18T00:00:00Z | ||
| datePublished | 2015-12-17T00:00:00Z |