By using five highly polymorphic markers, the allelic status of chromo
some 1 was established in a series of 236 tumors of the nervous system
, including all major histologic subtypes: gliomas, meningiomas, neuri
nomas, neuroblastomas, medulloblastomas, etc. Loss of alleles at 1p wa
s observed at significant frequencies in neuroblastomas (26% of cases)
, meningiomas (32%), and malignant gliomas (37%) (primarily oligodendr
ogliomas [94%1]). This anomaly was also detected in two of 23 neurinom
as, two of three neurofibrosarcomas, one primary lymphoma, and two met
astatic tumors of the brain. The analysis of tumors displaying partial
1p deletions suggests the existence of two distinct regions, 1p36 and
1p35-p32, in which loci nonrandomly involved in the development of ne
urogenic neoplasms might be located.