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Items: 3

1.

Comparative genomic analyses of the human NPHP1 locus reveal complex genomic architecture and its regional evolution in primates

(Submitter supplied) Many loci in the human genome harbor complex genomic structures that can result in susceptibility to genomic rearrangements leading to various genomic disorders. Nephronophthisis 1 (NPHP1, MIM# 256100) is an autosomal recessive disorder that can be caused by defects of NPHP1; the gene maps within the human 2q13 region where low copy repeats (LCRs) are abundant. Loss of function of NPHP1 is responsible for approximately 85% of the NPHP1 cases - about 80% of such individuals carry a large recurrent homozygous NPHP1 deletion that occurs via non-allelic homologous recombination (NAHR) between two flanking directly oriented ~45 kb LCRs. more...
Organism:
Papio anubis; Macaca mulatta; Gorilla gorilla; Pongo abelii; Homo sapiens; Pan troglodytes
Type:
Genome variation profiling by genome tiling array
Platform:
GPL21019
32 Samples
Download data: TXT
Series
Accession:
GSE73962
ID:
200073962
2.

Agilent-032837 Homo sapiens 2q13_Pengfei

(Submitter supplied) Arrays of this design have barcodes that begin with 16032837 or 2532837. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent Feature Extraction feature number. more...
Organism:
Homo sapiens
1 Series
32 Samples
Download data: TXT
Platform
Accession:
GPL21019
ID:
100021019
3.

human Vs human Sample 10

Organism:
Homo sapiens
Source name:
H1-P208 (channel 1) NA10851 (channel 2)
Platform:
GPL21019
Series:
GSE73962
Download data: TXT
Sample
Accession:
GSM1906789
ID:
301906789
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