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Items: 5

1.

Recurrent 15q13 microdeletions

(Submitter supplied) We report a recurrent microdeletion syndrome causing mental retardation, epilepsy and variable facial and digital dysmorphisms. We describe nine patients, including six probands; two with de novo deletions, two who inherited the deletion from an affected parent, and two with unknown inheritance. The proximal breakpoint of the largest deletion is contiguous with breakpoint 3 (BP3) of the Prader-Willi/Angelman region extending 3.95 Mb distally to BP5. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
4 related Platforms
12 Samples
Download data: PAIR
Series
Accession:
GSE10189
ID:
200010189
2.

University of Washington Human Itsara PWS 388K custom design array, version 1

(Submitter supplied) Ultra high-density coverage of Prader-Willi region on chr15 Protocol: manufactured per NimbleGen protocol. The design utilized b35 coordinates, with 385,000 spaced over 15258127bp, corresponding to a final probe density of 1 oligo per 39 bp.
Organism:
Homo sapiens
1 Series
3 Samples
Download data
Platform
Accession:
GPL6380
ID:
100006380
3.

University of Washington Human original custom 2-plex 166K array, version 1

(Submitter supplied) per Nimblegen protocol
Organism:
Homo sapiens
1 Series
5 Samples
Download data
Platform
Accession:
GPL6345
ID:
100006345
4.

University of Washington Human custom 2-plex 166K array for 15q13 region, A2 subarray version 1

(Submitter supplied) per Nimblegen protocol
Organism:
Homo sapiens
1 Series
1 Sample
Download data
Platform
Accession:
GPL6343
ID:
100006343
5.

University of Washington Human custom 2-plex 166K array for 15q13 region, A1 version 1

(Submitter supplied) per Nimblegen protocol
Organism:
Homo sapiens
1 Series
3 Samples
Download data
Platform
Accession:
GPL6342
ID:
100006342
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