Array CGH or molecular karyotype 180 K

"""The CHG array (aCHG) or molecular karyotype is the diagnostic tool indicated in the case of patients with intellectual deficit, learning difficulties, mental retardation, autism, developmental disorders, multiple congenital anomalies, pathologies related to a high number of chromosomal rearrangements and copy number variations (CNVs). It has a high resolution throughout the genome that even allows rapid and reliable detection of losses and gains of small genetic material, impossible to detect with a conventional karyotype. In syndromic regions it presents an enlarged resolution. The 180K array has 180,000 probes and a resolution below 50 kb. It is capable of detecting more than 200 syndromes and mosaicisms in low percentages (>20%). Our service includes report of results and genetic counseling (before and after)."""