Microarray

ARUP offers oligonucleotide and SNP-based microarray technologies as a complement to classical cytogenetic techniques. Both technologies identify unbalanced chromosomal abnormalities (loss and/or gain of DNA) in patients with unexplained abnormal phenotypes such as mental retardation, developmental delay, dysmorphic features, congenital anomalies, and autism. SNP-based arrays will also identify long contiguous stretches of homozygosity which may suggest an increased likelihood for a recessive condition or uniparental disomy. Microarrays for specific disorders as well as prenatal microarrays for testing of amniotic fluid, chorionic villi (CVS), and products of conception specimens are also available.

New: Cytoscan HD Genome Browser

Test # Test Name Additional Information Test Keywords
2005763 Chromosome Analysis, Peripheral Blood, with Reflex to Genomic Microarray Constitutional Studies PB REFLEX, Turners, Klinefelter, Klinefelter's, Klinefelters, trisomy 13, mental retardation, developmental delay, 45X, 45,X, XXY, XYY, anomalies, birth defects, infertility
2005762 Chromosome Analysis, Products of Conception, with Reflex to Genomic Microarray Constitutional Studies POC REFLEX, Down, Downs, Down's, Trisomy 21, Trisomy 18, Turner, Turner's, Turners, Klinefelter, Klinefelter's, Klinefelters, trisomy 13, karyotype, prenatal, fetus, fetal, villi, placenta, pregnancy loss
2003414 Cytogenomic SNP Microarray Genomic Microarray CMA SNP, array, CGH, aCGH, CNV, mental retardation, developmental delay, anomalies, birth defects, CMA, snip, LOH, UPD, uniparental disomy
2006267 Cytogenomic SNP Microarray Buccal Sponge Genomic Microarray
2006325 Cytogenomic SNP Microarray—Oncology Technical Bulletin Genomic Microarray
2005633 Genomic SNP Microarray, Products of Conception Genomic Microarray ARRAY POC, conception, amnio, amniotic fluid, CVS, villi, cultured cells
2002366 Microarray Genomic, Fetal Genomic Microarray ARRAY FE, array, CGH, aCGH, CNV, ultrsound anomalies, birth defects, POC, products of conception, amnio, amniotic fluid, CVS, villi, cultured cells
2004434 X Chromosome Ultra-High Density Microarray, 954 Genes Genomic Microarray X ARRAY, Neurocognitive Impairments, X-linked, mental retardation, developmental delay, seizures, x chromosome
2002301 Microarray Family Study by FISH

Used to determine the presence of a known deletion or duplication, previously identified by microarray in a family member. If the original array was not performed at ARUP, contact an ARUP genetic counselor prior to sending the sample.

 		Please call a genetic counselor before ordering. Genomic Microarray (FISH) ARRAY FAM, Array, CGH, aCGH, parental
2006325 Cytogenomic SNP Microarray—Oncology Technical Bulletin Oncology Studies, Microarray